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

VORTECH'S PERSONAL DISPLAY SYSTEM

K Number: K913491 · Decision Sep 6, 1991
Classifications
1
FEI Numbers
163
Registration Numbers
163
Same Product Code
818
Applicant Total
11
Review Days
31

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Basic Information

Device Name
VORTECH'S PERSONAL DISPLAY SYSTEM
K Number
K913491
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1750
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Vortech Data, Inc.
Date Received
August 6, 1991
Decision Date
September 6, 1991
Product Code
JAK
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
JAK System, X-Ray, Tomography, Computed

Similar 510(k) Clearances

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

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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
K915362 VORTECH'S FILM DIGITIZER, FD-1
K914834 VORTECH 3M NETWORK PRINTING
K914444 XPR PRINTER REDUNDANCY
K914191 XLP NETWORK PRINTING
K915094 VORTECH'S IMAGE ARCHIVAL AND RETRIEVAL SYSTEM
K884434 VORTECH'S MEDICAL IMAGING GATEWAY
Search all 11 clearances from Vortech Data, Inc. →