Pilling Weck, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K990547PILLING WECK SURGICAL Y STENT FORCEPSApril 27, 1999
K974250VERSASTAT MULTIPOLAR SCISSORS AND CABLESFebruary 11, 1998
K962771BURKE CONGENITAL THORACOSCOPY INSTRUMENTSNovember 19, 1996
K945520HEMOCLIP ECOSYSTEMJanuary 27, 1995
K944552PILLING WECK M-20 DISPOSABLE AUTOMATIC HEMOCLIPNovember 7, 1994
K943719VISISTAT STAPLERAugust 24, 1994