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

PERSONAL DISPLAY SYSTEM

K Number: K924366 · Decision Apr 7, 1993
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
11
Review Days
222

Basic Information

Device Name
PERSONAL DISPLAY SYSTEM
K Number
K924366
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
VORTECH DATA, INC.
Date Received
August 28, 1992
Decision Date
April 7, 1993
Product Code
LLZ
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
LLZ System, Image Processing, Radiological

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Other Clearances by VORTECH DATA, INC.

K Number Device Name
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
K913491 VORTECH'S PERSONAL DISPLAY SYSTEM
K884434 VORTECH'S MEDICAL IMAGING GATEWAY
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