FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

MEDICAM

K Number: K820829 · Decision May 3, 1982
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
5
Applicant Total
11
Review Days
39

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Basic Information

Device Name
MEDICAM
K Number
K820829
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4160
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
M.P. Video, Inc.
Date Received
March 25, 1982
Decision Date
May 3, 1982
Product Code
FWB
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
FWB Camera, Television, Surgical, Without Audio

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FWB), ordered by most recent decision date.

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Other Clearances by M.P. Video, Inc.

K Number Device Name
K951386 COMBINATION CAMERA/LIGHT SOURCE
K943342 MEDICAM XENON LIGHT SOURCE
K942358 AUTOCLAVEABLE MEDICAM 900 DIGICON CAMERA
K941773 MEDICAM 900 REMOTE
K941693 MEDICAM ENDOCOUPLER AND BEAMSPLITTER
K893828 ML-800 AUTOELECTRONIC LIGHT SOURCE
K882924 MEDICAM MC-7 AND RP-7 SURGICAL CAMERAS
K871595 SURGICAL CAMERA ACCESSORIES
K871057 MC-SERIES SURGICAL CAMERAS
K871056 MEDICAM S-4 SURGICAL CAMERA
Search all 11 clearances from M.P. Video, Inc. →