AMIKACIN ELUTION DISK FOR AUTOBAC
FDA premarket approval N50485/S017 · decided 1988-04-05
Approval details
- PMA number
- N50485
- Supplement
- S017
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- AMIKACIN ELUTION DISK FOR AUTOBAC
- Generic name
- DISCS, ELUTION
- Applicant
- Organon Teknika Corp.
- Date received
- 1987-10-07
- Decision date
- 1988-04-05
- Days to decision
- 181 days
- Decision code
- APPR
- Product code
- LTX
- Advisory committee
- Microbiology
- Expedited review
- No
- Location
- Durham, NC
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| BACT/ALERT CSR (K003104) | Organon Teknika Corp. | 2000-10-20 |
| MDA D-DIMER (K000492) | Organon Teknika Corp. | 2000-06-07 |
| BACT/ALERT MB CULTURE BOTTLE (K000378) | Organon Teknika Corp. | 2000-03-02 |
| BACT/ALERT SV (K994343) | Organon Teknika Corp. | 2000-02-10 |
| BACT/ALERT SA (K993423) | Organon Teknika Corp. | 1999-12-15 |
| BACT/ALERT SN (K993421) | Organon Teknika Corp. | 1999-12-14 |
| BACT/ALERT MP PROCESS BOTTLE (K993576) | Organon Teknika Corp. | 1999-12-14 |
| BACT/ALERT FN (K992432) | Organon Teknika Corp. | 1999-09-24 |