Medical Device Manufacturer · US , Mchenry , IL

Edward Weck, Inc. - FDA 510(k) Cleared Devices

140 submissions · 140 cleared · Since 1976

140

Total

140

Cleared

Denied

Edward Weck, Inc. has 140 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 140 cleared submissions from 1976 to 1992. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Edward Weck, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Edward Weck, Inc.

140 devices

1-12 of 140

1 2 3 4

Cleared Jun 29, 1992

WECK TROCAR

K915378 · HET

Obstetrics & Gynecology · 213d

Cleared Mar 23, 1992

LM15(TM), CATALOG NUMBER - 523821

K914690 · GCJ

General & Plastic Surgery · 157d

Cleared Jan 09, 1992

HEMOCLIP II

K911915 · FZP

General & Plastic Surgery · 254d

Cleared Nov 29, 1991

PNEUMO-SEAL(TM)

K914470 · GCJ

General & Plastic Surgery · 53d

Cleared Jul 02, 1991

ENDOSCOPIC NEEDLHOLDER CAT. NUMBER 114705

K911272 · FHG

Obstetrics & Gynecology · 102d

Cleared Aug 06, 1990

HEM-O-LOK(TM)

K902108 · FZP

General & Plastic Surgery · 90d

Cleared Aug 02, 1990

WECK ELECTROSURGICAL GENERATOR #174200

K902232 · GEI

General & Plastic Surgery · 77d

Cleared Feb 15, 1990

BOWIE-DICK TEST CARD CATALOG NUMBER 008018

K897045 · JOJ

General Hospital · 58d

Cleared Aug 27, 1987

CORONARY ARTERY BYPASS GRAFT (CABG) MARKER

K871110 · DSY

Cardiovascular · 161d

Cleared Jul 02, 1985

AUTO/MANUAL TITANIUM HEMOCLIP LIGATING CLIP 527200

K851251 · FZP

General & Plastic Surgery · 97d

Cleared Jun 07, 1985

WECK LX TM SKIN STAPLER

K851258 · GAG

General & Plastic Surgery · 71d

Cleared Jan 23, 1985

HEMOCLIP X-20 AUTOMATIC HEMOCLIP LIGATING APPLIER

K844836 · GWD

Microbiology · 42d

1 2 3 4

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Edward Weck, Inc. - FDA 510(k) Cleared Devices

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