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

VIDEO PRINTER SYSTEM

K Number: K873419 · Decision Nov 2, 1987
Classifications
1
FEI Numbers
193
Registration Numbers
193
Same Product Code
17
Applicant Total
3
Review Days
68

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Basic Information

Device Name
VIDEO PRINTER SYSTEM
K Number
K873419
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4160
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Technology For Imaging, Inc.
Date Received
August 26, 1987
Decision Date
November 2, 1987
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

Similar 510(k) Clearances

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

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Other Clearances by Technology For Imaging, Inc.

K Number Device Name
K885183 ENDOSCOPIC LIGHT SOURCE
K863800 ENDOSCOPIC VIDEO CAMERA