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Keymed, Inc.

FDA Regulatory Profile

Keymed, Inc. appears in FDA public data with 0 recalls, 29 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Apr 22, 2010.

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Summary

Total Recalls
0
510(k) Clearances
29
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K100803OLYMPUS FLUSHING PUMP OFP MODEL: OFP-1Apr 22, 2010
K921179OLYMPUS-KEYMED DISINFECTANT FUME EXTRACTOR DFE-20Mar 29, 1993
K881004OLYMPUS-KEYMED ENDOSCOPIC CO2 REGULATOR, MODEL ECRMay 12, 1988
K861821KEYMED FIBERSCOPE AUTO DISINFECTORFeb 12, 1987
K864801THE KEYMED HI-LIGHT 250 LIGHT SOURCEDec 24, 1986
K862000KEYMED FLEXIBLE ESOPHAGEAL DILATORSAug 12, 1986
K860528THE KEYMED FIBERSCOPE STERILIZATION CASEJul 15, 1986
K861147UCS-2, ULTRASONIC CLEANING SOLUTIONJun 23, 1986
K860704THE KEYMED SIGMOIDOSCOPE DISINFECTION STANDJun 17, 1986
K851149KEY MED TRANSENDOSCOPIC VASCULAR DETECTOR TVD-1Nov 26, 1985
K854304KEYMED OFFICE COUCHNov 12, 1985
K853421THE KEYMED VARI-HEIGHT PATIENT COUCHSep 19, 1985
K841822KEYMED SIGMOIDOSCOPE SUCTION UNITJul 27, 1984
K841331OLYMPUS KC-10 MOBILE DISINFEC-STATJul 19, 1984
K841399BRONCHOSCOPE SUCTION UNITJul 18, 1984
K840920KEYMED MOBILE ENDOSCOPY PATIENT COUCHMar 19, 1984
K830586TRI-DILS-TRIPLE OLIVE-ESOPHAGEAL DILATORMar 24, 1983
K830247SPLIT COLON STIFFENING TUBEMar 15, 1983
K830026FIBERSCOPE DISINFECTANT IRRIGATORJan 14, 1983
K822401ST. MARK'S RECTAL BIOPSY FORCEPSAug 27, 1982

FDA data resources