Medical Device Manufacturer · US , Mchenry , IL

Surgikos, Inc. - FDA 510(k) Cleared Devices

56 submissions · 56 cleared · Since 1976

Total

Cleared

Denied

Surgikos, Inc. has 56 FDA 510(k) cleared general hospital devices. Based in Mchenry, US.

Historical record: 56 cleared submissions from 1976 to 1988.

Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Surgikos, Inc.

56 devices

1-12 of 56

Cleared Mar 21, 1988

HEALTH CARE EYE PROTECTION

K875107 · HOY

Ophthalmic · 98d

Cleared Dec 30, 1987

STERILE SURGICAL SCRUB BRUSH

K874653 · GEC

General & Plastic Surgery · 47d

Cleared May 30, 1986

NEUTRALON SURGICAL GLOVES

K861441 · KGO

General Hospital · 43d

Cleared Jul 23, 1985

BARRIER SURGICAL GOWN

K852870 · FYA

General Hospital · 15d

Cleared Sep 30, 1982

CIDEX*DIALYZER DISINFECTING SOLUTION

K822535 · FKQ

Chemistry · 37d

Cleared Jul 22, 1982

BARRIER ANTIMICROBIAL INCISE DRAPE

K820543 · KKX

General Hospital · 142d

Cleared Jun 02, 1982

SURGIKOS INCISE DRAPE

K820542 · KKX

General Hospital · 92d

Cleared Aug 20, 1981

BACTERICIDAL INCISE DRAPE

K811871 · KKX

General Hospital · 50d

Cleared Feb 23, 1981

SURGIKOS FACE MASK

K810316 · FXX

General Hospital · 17d

Cleared Aug 20, 1980

BARRIER TOWEL DRAPE

K801863 · KKX

General Hospital · 15d

Cleared Aug 20, 1980

BARRIER APERTURED DRAPE

K801864 · KKX

General Hospital · 15d

Cleared Feb 19, 1980

SURGIKOS NEUTRALON BR. SURGEON'S GLOVE

K800152 · KGO

General Hospital · 28d

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Surgikos, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Surgikos, Inc.

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