Ortho Pharmaceutical Corp.
Ortho Pharmaceutical Corp. appears in FDA public data with 0 recalls, 9 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on June 21, 1996.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 9
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K955648 | K-Y PERSONAL LUBRICANT | June 21, 1996 |
| K934516 | ADVANCE PREGNANCY TEST MODIFICATION | February 24, 1994 |
| K914990 | ADVANCE(R) PREGNANCY TEST | December 23, 1991 |
| K893488 | PULSATILE PUMP FOR GONADORELIN ACETATE | October 31, 1989 |
| K881151 | MICROSCRAPE | April 6, 1988 |
| K810581 | FACT* HOME PREGNANCY TEST | March 17, 1981 |
| K800754 | NICKERSON'S MED. SELECTIVE CULTURE MEDIU | April 29, 1980 |
| K792634 | CONCEPTROL/THIN PROPHYLACTICS | January 16, 1980 |
| K790087 | LUBRICANT, OTRHO PERSONAL | February 1, 1979 |