Medical Device Manufacturer · US , Walker , MI

Omega-Med Intl., Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1981

Total

Cleared

Denied

Omega-Med Intl., Inc. has 9 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 9 cleared submissions from 1981 to 1984. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Omega-Med Intl., Inc. Filter by specialty or product code using the sidebar.

Omega-Med Intl., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Omega-Med Intl., Inc.

9 devices

1-9 of 9

Cleared Sep 05, 1984

OMED DISPOS. INSTRUMENT GUARDS

K842603

General & Plastic Surgery · 62d

Cleared Mar 05, 1984

SUTURE-AID BOOTIES

K832441 · KDC

General & Plastic Surgery · 224d

Cleared Mar 24, 1983

OMED IDENT-I-BAND

K830484

General & Plastic Surgery · 37d

Cleared Sep 17, 1982

COMPLY NEUROMUSCULAR STIMULATOR

K822284 · IPF

Physical Medicine · 49d

Cleared May 24, 1982

OMED FABRIC INSTRUMENT COVERS-RADIOPAQ

K821334

General & Plastic Surgery · 19d

Cleared Dec 29, 1981

OMED DISPOSABLE BULLDOG

K813499 · DXC

Cardiovascular · 15d

Cleared Apr 23, 1981

OMED SILICONE INSTRUMENT COVERS

K810883 · KDC

General & Plastic Surgery · 22d

Cleared Feb 26, 1981

OMED SILICONE LOOPS

K810260 · KDC

General & Plastic Surgery · 27d

Cleared Feb 26, 1981

OMED FABRIC INSTRUMENT COVERS

K810269 · KDC

General & Plastic Surgery · 24d

Omega-Med Intl., Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Omega-Med Intl., Inc.

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