Anarobe Systems
Anarobe Systems appears in FDA public data with 0 recalls, 7 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on August 17, 1984.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K842850 | TRIPLE SUGAR IRON | August 17, 1984 |
| K842854 | MUELLER HINTON BROTH | August 17, 1984 |
| K842851 | ORNITHINE INDOLE MOTILITY | August 7, 1984 |
| K842849 | TRYPTICASE SOY BROTH | August 3, 1984 |
| K842853 | LYSINE IRON AGAR | August 3, 1984 |
| K842855 | CHRISTENSEN'S UREA AGAR | August 3, 1984 |
| K842852 | BRAIN HEART INFUSION BROTH | August 3, 1984 |