FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

KEYMED SIGMOIDOSCOPE SUCTION UNIT

K Number: K841822 · Decision Jul 27, 1984
Classifications
1
FEI Numbers
13
Registration Numbers
13
Same Product Code
44
Applicant Total
29
Review Days
86

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Basic Information

Device Name
KEYMED SIGMOIDOSCOPE SUCTION UNIT
K Number
K841822
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.5200
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Keymed, Inc.
Date Received
May 2, 1984
Decision Date
July 27, 1984
Product Code
DRM
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DRM Compressor, Cardiac, External

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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
K864801 THE KEYMED HI-LIGHT 250 LIGHT SOURCE
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
Search all 29 clearances from Keymed, Inc. →