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

UPSCAN

K Number: K933512 · Decision Apr 19, 1995
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
355
Applicant Total
8
Review Days
638

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Basic Information

Device Name
UPSCAN
K Number
K933512
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1680
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Merlin Engineering Works, Inc.
Date Received
July 20, 1993
Decision Date
April 19, 1995
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

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

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Other Clearances by Merlin Engineering Works, Inc.

K Number Device Name
K974882 DOWNSCAN LT
K971153 SPLITSCREEN (ME-975)
K971154 MULTIPICS(ME-977)
K970451 DOWNSCAN 120
K970450 UPSCAN 120
K954211 CRISPICS
K953398 UNISCAN