FDA 510(k) FDA class 2 Substantially Equivalent 🇬🇧 United Kingdom

THE KEYMED HI-LIGHT 250 LIGHT SOURCE

K Number: K864801 · Decision Dec 24, 1986
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
46
Applicant Total
29
Review Days
15

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Basic Information

Device Name
THE KEYMED HI-LIGHT 250 LIGHT SOURCE
K Number
K864801
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Keymed, Inc.
Date Received
December 9, 1986
Decision Date
December 24, 1986
Product Code
GCT
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GCT Light Source, Endoscope, Xenon Arc

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Other Clearances by Keymed, Inc.

K Number Device Name
K100803 OLYMPUS FLUSHING PUMP OFP MODEL: OFP-1
K921179 OLYMPUS-KEYMED DISINFECTANT FUME EXTRACTOR DFE-20
K881004 OLYMPUS-KEYMED ENDOSCOPIC CO2 REGULATOR, MODEL ECR
K861821 KEYMED FIBERSCOPE AUTO DISINFECTOR
K862000 KEYMED FLEXIBLE ESOPHAGEAL DILATORS
K860528 THE KEYMED FIBERSCOPE STERILIZATION CASE
K861147 UCS-2, ULTRASONIC CLEANING SOLUTION
K860704 THE KEYMED SIGMOIDOSCOPE DISINFECTION STAND
K851149 KEY MED TRANSENDOSCOPIC VASCULAR DETECTOR TVD-1
K854304 KEYMED OFFICE COUCH
Search all 29 clearances from Keymed, Inc. →