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

VIDEO PLUS WITH ANALYTICAL WORKSTATION

K Number: K941979 · Decision Aug 17, 1994
Classifications
1
FEI Numbers
123
Registration Numbers
123
Same Product Code
198
Applicant Total
16
Review Days
114

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Basic Information

Device Name
VIDEO PLUS WITH ANALYTICAL WORKSTATION
K Number
K941979
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1600
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Camtronics, Ltd.
Date Received
April 25, 1994
Decision Date
August 17, 1994
Product Code
IZI
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
IZI System, X-Ray, Angiographic

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (IZI), 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. →