Medical Device Manufacturer · US , Mchenry , IL

Surgi-Quip Inc.U - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1982

8

Total

8

Cleared

0

Denied

Surgi-Quip Inc.U has 8 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 8 cleared submissions from 1982 to 1984. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Surgi-Quip Inc.U Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Surgi-Quip Inc.U

8 devices

1-8 of 8

Cleared May 09, 1984

CHARLES/MCINTYRE GIANT BREAK TABLE

General & Plastic Surgery · 55d

Cleared May 09, 1984

MOBILE OPHTHALMIC OPERATING TABLE

General & Plastic Surgery · 55d

Cleared Mar 22, 1984

WEE BAG O'MERCURY

Ophthalmic · 78d

Cleared Oct 04, 1983

ELECTRONIC UNIT

General & Plastic Surgery · 39d

Cleared Sep 14, 1982

SELF-CONTAINED MOBILE OPHTHAL. OPER. .

General & Plastic Surgery · 33d

Cleared Sep 14, 1982

CEMENT EXTRACTION INSTRUMENTATION

General & Plastic Surgery · 21d

Cleared Sep 02, 1982

MCINTYRE MICROSCOPE STAND

Pathology · 21d

Cleared Sep 02, 1982

SURGI-QUIP MICROSCOPE STAND

Pathology · 21d