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

VORTECH'S FILM DIGITIZER, FD-1

K Number: K915362 · Decision Apr 6, 1992
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
355
Applicant Total
11
Review Days
131

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Basic Information

Device Name
VORTECH'S FILM DIGITIZER, FD-1
K Number
K915362
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1680
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Vortech Data, Inc.
Date Received
November 27, 1991
Decision Date
April 6, 1992
Product Code
KPR
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
KPR System, X-Ray, Stationary

Similar 510(k) Clearances

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Other Clearances by Vortech Data, Inc.

K Number Device Name
K924366 PERSONAL DISPLAY SYSTEM
K925097 VORTECH'S AUTOROUTER (AUTOMATIC IMAGE ROUTING)
K924229 VG-A MIG
K922310 VORTECH'S PERSONAL DISPLAY SYSTEM
K914834 VORTECH 3M NETWORK PRINTING
K914444 XPR PRINTER REDUNDANCY
K914191 XLP NETWORK PRINTING
K915094 VORTECH'S IMAGE ARCHIVAL AND RETRIEVAL SYSTEM
K913491 VORTECH'S PERSONAL DISPLAY SYSTEM
K884434 VORTECH'S MEDICAL IMAGING GATEWAY
Search all 11 clearances from Vortech Data, Inc. →