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

BRAINLAB LINAC HARDWARE

K Number: K934657 · Decision Jul 22, 1994
Classifications
1
FEI Numbers
123
Registration Numbers
124
Same Product Code
717
Applicant Total
5
Review Days
304

Basic Information

Device Name
BRAINLAB LINAC HARDWARE
K Number
K934657
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
BRAINLAB MED. COMPUTERSYSTEME GMBH
Date Received
September 21, 1993
Decision Date
July 22, 1994
Product Code
IYE
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
IYE Accelerator, Linear, Medical

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