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

DIGITAL ADD ON MULTI SYSTEM

K Number: K973710 · Decision Dec 18, 1997
Classifications
1
FEI Numbers
84
Registration Numbers
84
Same Product Code
347
Applicant Total
3
Review Days
80

Basic Information

Device Name
DIGITAL ADD ON MULTI SYSTEM
K Number
K973710
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1680
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
SWISSRAY INTERNATIONAL, INC.
Date Received
September 29, 1997
Decision Date
December 18, 1997
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

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