510(k) K946053

Device
SIMVIEW(TM) 3000
Applicant
Siemens Medical Solutions USA, Inc.
510(k) number
K946053
Product code
KPQ
Decision
Substantially Equivalent (SESE)
Decision date
1995-03-31
Date received
1994-12-12
Regulation
892.5840
Classification name
System, Simulation, Radiation Therapy
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
KENNETH R MICHAEL
Address
4040 Nelson Ave. Concord CA US 94520 94520

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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