Progensa PCA3 Assay
FDA premarket approval P100033/S009 · decided 2018-10-18
Approval details
- PMA number
- P100033
- Supplement
- S009
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- Progensa PCA3 Assay
- Generic name
- Prostrate cancer genes nucleic acid amplification test system
- Applicant
- Gen-Probe Incorporated
- Date received
- 2018-09-25
- Decision date
- 2018-10-18
- Days to decision
- 23 days
- Decision code
- OK30
- Product code
- OYM
- Advisory committee
- Pathology
- Expedited review
- No
- Location
- San Diego, CA
- Statement
- Remove an in-process performance test that is no longer applicable to currently marketed products.
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| APTIMA TRICHOMONAS VAGINALIS ASSAY (DEN110012) | Gen-Probe Incorporated | 2011-04-19 |