UROVYSION BLADDER CANCER KIT
FDA premarket approval P030052/S018 · decided 2016-09-29
Approval details
- PMA number
- P030052
- Supplement
- S018
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- UROVYSION BLADDER CANCER KIT
- Applicant
- Abbott Molecular
- Date received
- 2016-09-02
- Decision date
- 2016-09-29
- Days to decision
- 27 days
- Decision code
- OK30
- Advisory committee
- Pathology
- Expedited review
- No
- Location
- Des Plaines, IL
- Statement
- Location change for a component supplier.
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| simpli-COLLECT STI Test (K243410) | Abbott Molecular | 2025-01-30 |
| Alinity m SARS-CoV-2 AMP Kit (09N78-096); Alinity m SARS-CoV-2 CTRL Kit (09N78-086) (K241580) | Abbott Molecular | 2024-12-06 |