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
K844836HEMOCLIP X-20 AUTOMATIC HEMOCLIP LIGATING APPLIERJanuary 23, 1985
K844837VISISTAT SKIN STAPLING DEVICEJanuary 23, 1985
K844838SKIN STAT II SKIN STAPLING MEDICAL DEVICEJanuary 23, 1985
K841548HEMOCLIP LIGATING CLIPS M/LARGEAugust 14, 1984
K841547HEMOCLIP LIGATING CLIPS MED/SMLAugust 14, 1984
K841549HEMOCLIP AUTOMATIC CLIPS MEDIUMAugust 14, 1984
K833646PULSATRON NERVE LOCATOR/STIMULATORFebruary 10, 1984
K833648OPHTHALMIC CAUTERY #6821-HOT-TEMP #'SNovember 29, 1983
K832795HEIFETZ INTRACRANIAL ANEURYSM CLIPSNovember 25, 1983