Omni Mfg., Inc.
Omni Mfg., Inc. appears in FDA public data with 0 recalls, 1 510(k) clearance, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on June 24, 1993.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 1
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K931610 | OMNISORB II, NONWOVEN SPONGE, STERILE AND NON | June 24, 1993 |