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

SIRESKOP CX

K Number: K932445 · Decision Sep 7, 1993
Classifications
1
FEI Numbers
139
Registration Numbers
139
Same Product Code
297
Applicant Total
519
Review Days
110

Basic Information

Device Name
SIRESKOP CX
K Number
K932445
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1650
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
Date Received
May 20, 1993
Decision Date
September 7, 1993
Product Code
JAA
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
JAA System, X-Ray, Fluoroscopic, Image-Intensified

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