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

VIDEO PLUS MODELS VP500, VP500A AND VP1000

K Number: K871743 · Decision Jun 22, 1987
Classifications
1
FEI Numbers
136
Registration Numbers
136
Same Product Code
299
Applicant Total
16
Review Days
48

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Basic Information

Device Name
VIDEO PLUS MODELS VP500, VP500A AND VP1000
K Number
K871743
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1650
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Camtronics, Ltd.
Date Received
May 5, 1987
Decision Date
June 22, 1987
Product Code
JAA
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
JAA System, X-Ray, Fluoroscopic, Image-Intensified

Similar 510(k) Clearances

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

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Other Clearances by Camtronics, Ltd.

K Number Device Name
K021236 SURGERY AND ACCESSORIES
K013032 PHYSIOLOG, SERIES 95000
K992666 VIDEO PLUS SYSTEM, SERIES 95000
K992259 ECHOCARDIOGRAPHY SYSTEM SERIES 95000
K990066 CCD CAMERA, MODEL 9000
K955519 ANALYTICAL REVIEW STATION
K954159 DIGITAL IMAGING SYSTEM
K955232 NT SERIES DIGITAL IMAGE MANAGER
K953080 DIGITAL IMAGING SYSTEM INTERFACE
K945654 NICOM DIGITAL IMAGE MANAGER
Search all 16 clearances from Camtronics, Ltd. →