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

AX WORKSTATION DR-VIEWER SOFTWARE OPTION

K Number: K992925 · Decision Nov 23, 1999
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
66
Review Days
85

Basic Information

Device Name
AX WORKSTATION DR-VIEWER SOFTWARE OPTION
K Number
K992925
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SIEMENS CORP.
Date Received
August 30, 1999
Decision Date
November 23, 1999
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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