Ortho Pharmaceutical Corp.
FDA 510(k) & PMA Approved Devices — 9 products
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Total Devices9
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K955648 | K-Y PERSONAL LUBRICANT | HIS | 1996-06-21 | View |
| 510(k) | K934516 | ADVANCE PREGNANCY TEST MODIFICATION | LCX | 1994-02-24 | View |
| 510(k) | K914990 | ADVANCE(R) PREGNANCY TEST | LCX | 1991-12-23 | View |
| 510(k) | K893488 | PULSATILE PUMP FOR GONADORELIN ACETATE | FRN | 1989-10-31 | View |
| 510(k) | K881151 | MICROSCRAPE | LXK | 1988-04-06 | View |
| 510(k) | K810581 | FACT* HOME PREGNANCY TEST | JHJ | 1981-03-17 | View |
| 510(k) | K800754 | NICKERSON'S MED. SELECTIVE CULTURE MEDIU | JSJ | 1980-04-29 | View |
| 510(k) | K792634 | CONCEPTROL/THIN PROPHYLACTICS | HIS | 1980-01-16 | View |
| 510(k) | K790087 | LUBRICANT, OTRHO PERSONAL | KMJ | 1979-02-01 | View |
No matching devices.
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