ElintMAX Respiratory Monitor (ElintMAX Monitor A1) (K260226): 510(k) cleared for Amptron Medical, Inc.
ElintMAX Respiratory Monitor (ElintMAX Monitor A1) (K260226): 510(k) cleared for Amptron Medical, Inc. (California): 510(k) cleared for Amptron Medical, Inc. Its amount of 233 is above the median of 138 (74th percentile). Dated 50 days ago, it serves as a historical benchmark. Score 42/100. As of 2026-11-04, from U.S. FDA openFDA (510(k) clearances and device enforcement reports).
Data as of · Compiled by Zalwin from U.S. FDA openFDA (510(k) clearances and device enforcement reports)
amount: 233 · 74th percentile of 414 FDAPulse records · 1.7x the median
Free preview: all 14 published fields of this record are shown below. Locked: 75 related CA FDAPulse records and the 5-column CSV export.
| Field | Value |
|---|---|
| Record | 510(k) clearance |
| 510(k) number | K260226 |
| Device | ElintMAX Respiratory Monitor (ElintMAX Monitor A1) |
| Applicant | Amptron Medical, Inc. |
| Specialty / panel | Anesthesiology |
| Product code | BZK |
| Device class | 2 |
| Clearance type | Traditional |
| Decision | Substantially Equivalent |
| Received | 2026-01-26 |
| Decision date | 2026-09-16 |
| Review time (days) | 233 |
| Third-party review | No |
| Applicant location | Carlsbad, CA, US |
| amount percentile | 74th of 414 (median 138, 1.7x median) |
| Peer records CSV (76 CA records) | 🔒 Click to unlock → |
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CSV columns: Record · Specialty · Date · Review days · Recall class · official source URL
- Source agency: U.S. FDA openFDA (510(k) clearances and device enforcement reports)
- Record date: 2026-09-16
- Data refreshed: 2026-11-04
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Top FDAPulse records (CA first): Triever Duo Catheter (K253419) · Helo Return (K253717) · DistaSense(TM) (v1) (K254058) · BD OneFlow LST; BD OneFlow B-CLPD T1; BD FACSLyric Flow Cyto · CapsoView (CVV); CapsoCloud (CLD) (K254230) · Browse all by state and category →
LIVE PUBLIC DATA Source: U.S. FDA openFDA (510(k) clearances and device enforcement reports) · Last refreshed: Wed, 04 Nov 2026 21:30:53 GMT
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Peer benchmark and outreach value: ElintMAX Respiratory Monitor (ElintMAX Monitor A1) (K260226): 510(k) cleared for Amptron Medical, Inc. and 76 California peers
- California FDAPulse records like this one: 76
- ElintMAX Respiratory Monitor (ElintMAX Monitor A1) (K260226): 510(k) cleared for Amptron Medical, Inc.'s amount: 74th percentile of 414 records
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every California peer: $15,200 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
42 / 100 Predicate Speed & CAPA Advisory Opportunity Score
- 233-day review, longer than typical.
What is the FDAPulse record for ElintMAX Respiratory Monitor (ElintMAX Monitor A1) (K260226): 510(k) cleared for Amptron Medical, Inc. in California?
ElintMAX Respiratory Monitor (ElintMAX Monitor A1) (K260226) by Amptron Medical, Inc. was cleared on 2026-09-16 after 233 days of review.
How does ElintMAX Respiratory Monitor (ElintMAX Monitor A1) (K260226): 510(k) cleared for Amptron Medical, Inc. compare to other California FDAPulse records?
Its amount of 233 sits in the upper half (74th percentile) of 414 records; the median is 138. It is 50 days old; check the official source for later updates before acting.
ElintMAX Respiratory Monitor (ElintMAX Monitor A1) (K260226) vs. top 3 peers
| Organization | Location | Record date |
|---|---|---|
| ElintMAX Respiratory Monitor (ElintMAX Monitor A1) (K260226) | CA | 2026-09-16 |
| BreathCare PAP III (YH-390N) (K260251) | CN | 2026-10-23 |
| Helo Return (K253717) | CA | 2026-10-11 |
| Aevice Wheeze Detection Module (K260140) | SG | 2026-09-25 |
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