Medical Device Manufacturer · US , Mchenry , IL

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

29 submissions · 29 cleared · Since 1981

Total

Cleared

Denied

Keymed, Inc. has 29 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 29 cleared submissions from 1981 to 2010. Primary specialty: General Hospital.

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

Keymed, 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 - Keymed, Inc.

29 devices

1-12 of 29

Cleared Apr 22, 2010

OLYMPUS FLUSHING PUMP OFP MODEL: OFP-1

K100803 · FEQ

Gastroenterology & Urology · 31d

Cleared Mar 29, 1993

OLYMPUS-KEYMED DISINFECTANT FUME EXTRACTOR DFE-20

K921179 · FEB

General Hospital · 385d

Cleared May 12, 1988

OLYMPUS-KEYMED ENDOSCOPIC CO2 REGULATOR, MODEL ECR

K881004 · FCX

Gastroenterology & Urology · 64d

Cleared Feb 12, 1987

KEYMED FIBERSCOPE AUTO DISINFECTOR

K861821 · NVE

General Hospital · 276d

Cleared Dec 24, 1986

THE KEYMED HI-LIGHT 250 LIGHT SOURCE

K864801 · GCT

Gastroenterology & Urology · 15d

Cleared Aug 12, 1986

KEYMED FLEXIBLE ESOPHAGEAL DILATORS

K862000 · KNQ

Gastroenterology & Urology · 81d

Cleared Jul 15, 1986

THE KEYMED FIBERSCOPE STERILIZATION CASE

K860528 · KCT

General Hospital · 154d

Cleared Jun 23, 1986

UCS-2, ULTRASONIC CLEANING SOLUTION

K861147 · FLG

General Hospital · 89d

Cleared Jun 17, 1986

THE KEYMED SIGMOIDOSCOPE DISINFECTION STAND

K860704 · NZA

General Hospital · 111d

Cleared Nov 26, 1985

KEY MED TRANSENDOSCOPIC VASCULAR DETECTOR TVD-1

General Hospital · 18d

Cleared Sep 19, 1985

THE KEYMED VARI-HEIGHT PATIENT COUCH

K853421 · FPO

General Hospital · 36d

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

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

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