Edward Weck, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
140
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K915378WECK TROCARJune 29, 1992
K914690LM15(TM), CATALOG NUMBER - 523821March 23, 1992
K911915HEMOCLIP IIJanuary 9, 1992
K914470PNEUMO-SEAL(TM)November 29, 1991
K911272ENDOSCOPIC NEEDLHOLDER CAT. NUMBER 114705July 2, 1991
K902108HEM-O-LOK(TM)August 6, 1990
K902232WECK ELECTROSURGICAL GENERATOR #174200August 2, 1990
K897045BOWIE-DICK TEST CARD CATALOG NUMBER 008018February 15, 1990
K871110CORONARY ARTERY BYPASS GRAFT (CABG) MARKERAugust 27, 1987
K851251AUTO/MANUAL TITANIUM HEMOCLIP LIGATING CLIP 527200July 2, 1985
K851258WECK LX TM SKIN STAPLERJune 7, 1985
K844838SKIN STAT II SKIN STAPLING MEDICAL DEVICEJanuary 23, 1985
K844837VISISTAT SKIN STAPLING DEVICEJanuary 23, 1985
K844836HEMOCLIP X-20 AUTOMATIC HEMOCLIP LIGATING APPLIERJanuary 23, 1985
K841548HEMOCLIP LIGATING CLIPS M/LARGEAugust 14, 1984
K841549HEMOCLIP AUTOMATIC CLIPS MEDIUMAugust 14, 1984
K841547HEMOCLIP LIGATING CLIPS MED/SMLAugust 14, 1984
K833646PULSATRON NERVE LOCATOR/STIMULATORFebruary 10, 1984
K833648OPHTHALMIC CAUTERY #6821-HOT-TEMP #'SNovember 29, 1983
K832795HEIFETZ INTRACRANIAL ANEURYSM CLIPSNovember 25, 1983