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

SIENET DIAGNOSTIC REPORTING CONSOLE

K Number: K920309 · Decision Mar 20, 1992
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
53
Review Days
57

Basic Information

Device Name
SIENET DIAGNOSTIC REPORTING CONSOLE
K Number
K920309
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SIEMENS GAMMASONICS, INC.
Date Received
January 23, 1992
Decision Date
March 20, 1992
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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K922373 MULTISPECT(TM) 2 DUAL DETECTOR CAMERA SYSTEM
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