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

SONY VIDEO PRINTERS, UP SERIES

K Number: K882958 · Decision Aug 4, 1988
Classifications
1
FEI Numbers
193
Registration Numbers
193
Same Product Code
17
Applicant Total
8
Review Days
21

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Basic Information

Device Name
SONY VIDEO PRINTERS, UP SERIES
K Number
K882958
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4160
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Sony Medical Electronics Co.
Date Received
July 14, 1988
Decision Date
August 4, 1988
Product Code
KQM
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
KQM Camera, Surgical And Accessories

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Other Clearances by Sony Medical Electronics Co.

K Number Device Name
K980279 SONY DXC-LS1 COLOR VIDEO CAMERA
K913886 SONY DVR-10 DIGITAL VIDEOCASSETTE RECORDER
K904447 SONY CINE VIDEO SYSTEM SME-3500
K902535 SONY WBS-700H VIDEOCASSETTE RECORDER SYSTEM
K901153 SONY VO-5800H VIDEOCASSETTE RECORDER
K885042 SONY TRINITRON COLOR VIDEO MONITOR PVM-1343MD
K884008 SONY CINE VIDEO SYSTEM SME-3300