Univec, Inc.
Univec, Inc. 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 March 19, 2002.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K020500 | UNIVEC BIFURCATED SLIDING SHEATH SYRINGE | March 19, 2002 |
| K993996 | UNIVEC AUTO-DISABLE HYPODERMIC SYRINGE | July 17, 2000 |
| K000747 | UNIVEC TWO PIECE SYRINGE | June 8, 2000 |
| K961877 | PISTON SYRINGE | August 7, 1996 |
| K933469 | UNIVEC NON-REUSABLE SYRINGE | April 18, 1996 |
| K951619 | UNIVEC NONREUSABLE LOCKING SYRINGE | June 6, 1995 |
| K943679 | UNIVEC NONRESUSABLE LOCKING SYRINGE | December 12, 1994 |