Medical Device Manufacturer · US , Mchenry , IL

I M, Inc. - FDA 510(k) Cleared Devices

41 submissions · 40 cleared · Since 1976

Total

Cleared

Denied

I M, Inc. has 40 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 40 cleared submissions from 1976 to 1992.

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

I M, 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 - I M, Inc.

41 devices

1-12 of 41

General & Plastic Surgery · 101d

Cleared Jun 23, 1988

SYRINGE PREFILLED WITH WATER

K881363 · KOD

Gastroenterology & Urology · 84d

Cleared Apr 27, 1988

UMBILICAL CORD CLAMP

K880753 · HFW

Obstetrics & Gynecology · 62d

Cleared Oct 20, 1987

NUTRIPUMP

K872741 · FRN

General Hospital · 102d

Cleared May 08, 1987

BANDAGES CATALOG NUMBER: 101 TO 220

K871495 · NAD

General & Plastic Surgery · 22d

Cleared Dec 11, 1986

MAKLER CATHETER

K863785 · HDR

Obstetrics & Gynecology · 76d

Cleared Dec 10, 1985

STERILE SALINE SOLUTION

K854155 · KMJ

General Hospital · 60d

Cleared Oct 17, 1985

HUBOUT

K853287 · FPA

General Hospital · 73d

Cleared Oct 04, 1985

FEEDING UNITS & TUBES

K853288 · KNT

Gastroenterology & Urology · 38d

Cleared Aug 21, 1985

STAPLE REMOVER

K853286

General & Plastic Surgery · 16d

Cleared Jan 18, 1985

FORCEPS & HAMOSTATS

K844062 · GEN

General & Plastic Surgery · 92d

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I M, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - I M, Inc.

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