Keymed, Inc. - FDA 510(k) Cleared Devices
29
Total
29
Cleared
0
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.
29 devices
Cleared
Apr 22, 2010
OLYMPUS FLUSHING PUMP OFP MODEL: OFP-1
Gastroenterology & Urology
31d
Cleared
Mar 29, 1993
OLYMPUS-KEYMED DISINFECTANT FUME EXTRACTOR DFE-20
General Hospital
385d
Cleared
May 12, 1988
OLYMPUS-KEYMED ENDOSCOPIC CO2 REGULATOR, MODEL ECR
Gastroenterology & Urology
64d
Cleared
Feb 12, 1987
KEYMED FIBERSCOPE AUTO DISINFECTOR
General Hospital
276d
Cleared
Dec 24, 1986
THE KEYMED HI-LIGHT 250 LIGHT SOURCE
Gastroenterology & Urology
15d
Cleared
Aug 12, 1986
KEYMED FLEXIBLE ESOPHAGEAL DILATORS
Gastroenterology & Urology
81d
Cleared
Jul 15, 1986
THE KEYMED FIBERSCOPE STERILIZATION CASE
General Hospital
154d
Cleared
Jun 23, 1986
UCS-2, ULTRASONIC CLEANING SOLUTION
General Hospital
89d
Cleared
Jun 17, 1986
THE KEYMED SIGMOIDOSCOPE DISINFECTION STAND
General Hospital
111d
Cleared
Nov 26, 1985
KEY MED TRANSENDOSCOPIC VASCULAR DETECTOR TVD-1
Radiology
250d
Cleared
Nov 12, 1985
KEYMED OFFICE COUCH
General Hospital
18d
Cleared
Sep 19, 1985
THE KEYMED VARI-HEIGHT PATIENT COUCH
General Hospital
36d