Atlas FDA

MEDICAM

FDA 510(k) clearance K820829 · decided 1982-05-03

Clearance details

K-number
K820829
Device name
MEDICAM
Applicant
M.P. Video, Inc.
Decision
Substantially Equivalent
Date received
1982-03-25
Decision date
1982-05-03
Days to decision
39 days
Clearance type
Traditional
Product code
FWB
Device class
1
Regulation number
878.4160
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
CAMERA, SURGICAL AND ACCESSORIES (K934092)Envision Medical Corp.1994-01-07
SURGICAL VIDEO CAMERA, MODEL 9500 (K902359)Seitz Technical Products, Inc.1990-07-12
SONY COLOR VIDEO CAMERAS AND ACCESSORIES (K884343)Sony Corp. of America1988-11-01
MC-SERIES SURGICAL CAMERAS (K871057)M.P. Video, Inc.1987-04-03
MEDICAL DYNAMICS CCD SOLID STATE VIDEO CAMERA 5930 (K855020)Medline Industries, Inc.1986-01-24

Recalls involving this device

No recalls on record reference this clearance.