Agilent Technologies, Inc.: PMA supplement approved for PD-L1 IHC 28-8 pharmDx
Agilent Technologies, Inc. (Santa Clara, California): PMA supplement approved for PD-L1 IHC 28-8 pharmDx. Dated 127 days ago, it serves as a historical benchmark. Score 30/100. As of 2026-11-04, from openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration).
Data as of · Compiled by Zalwin from openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration)
Free preview: all 8 published fields of this record are shown below. Locked: 109 related CA FdaApprovalPulse records and the 4-column CSV export.
| Field | Value |
|---|---|
| Sponsor | Agilent Technologies, Inc. |
| Product | PD-L1 IHC 28-8 pharmDx |
| Generic / ingredient | Immunohistochemistry assay, antibody, programmed death-ligand 1 |
| Approval | PMA supplement (device change) |
| Application | P150025 S018 |
| Decided | 2026-07-01 |
| Panel / class | Pathology |
| Sponsor location | Santa Clara, CA |
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CSV columns: Sponsor · Product · Approval · Decided · official source URL
- Source agency: openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration)
- Record date: 2026-07-01
- Data refreshed: 2026-11-04
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LIVE PUBLIC DATA Source: openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration) · Last refreshed: Wed, 04 Nov 2026 06:06:18 GMT
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Peer benchmark and outreach value: Agilent Technologies, Inc. and 110 California peers
- California FdaApprovalPulse records like this one: 110
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every California peer: $22,000 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
30 / 100 Score
What is the FdaApprovalPulse record for Agilent Technologies, Inc. in Santa Clara, California?
The FDA approved PD-L1 IHC 28-8 pharmDx (P150025 S018) for Agilent Technologies, Inc. on 2026-07-01: PMA supplement (device change).
How does Agilent Technologies, Inc. compare to other California FdaApprovalPulse records?
It is 127 days old; check the official source for later updates before acting. Its Score of 30/100 is modest; treat it as background rather than a priority.
Agilent Technologies, Inc. vs. top 3 peers
| Organization | Location | Record date |
|---|---|---|
| Agilent Technologies, Inc. | Santa Clara, CA | 2026-07-01 |
| Edwards Lifesciences, LLC | Irvine, CA | 2026-10-22 |
| Edwards Lifesciences, LLC | Irvine, CA | 2026-10-22 |
| Edwards Lifesciences, LLC | Irvine, CA | 2026-10-22 |
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From openFDA (PMA and Drugs@FDA). openFDA can lag FDA decisions by days to weeks. Drug supplement types follow the FDA submission class (labeling and REMS, manufacturing/CMC, efficacy, other). Company and product level only. Verify on FDA databases before relying on an approval.