Univec, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K020500UNIVEC BIFURCATED SLIDING SHEATH SYRINGEMarch 19, 2002
K993996UNIVEC AUTO-DISABLE HYPODERMIC SYRINGEJuly 17, 2000
K000747UNIVEC TWO PIECE SYRINGEJune 8, 2000
K961877PISTON SYRINGEAugust 7, 1996
K933469UNIVEC NON-REUSABLE SYRINGEApril 18, 1996
K951619UNIVEC NONREUSABLE LOCKING SYRINGEJune 6, 1995
K943679UNIVEC NONRESUSABLE LOCKING SYRINGEDecember 12, 1994