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FDA 510(k) Application Details - K940663
Device Classification Name
Accelerator, Linear, Medical
More FDA Info for this Device
510(K) Number
K940663
Device Name
Accelerator, Linear, Medical
Applicant
NOMOS CORP.
2593 WEXFORD BAYNE RD.
SUITE 315
SEWICKLEY, PA 15143 US
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Contact
HARRIS S TARGOVNIK, PH.D.
Other 510(k) Applications for this Contact
Regulation Number
892.5050
More FDA Info for this Regulation Number
Classification Product Code
IYE
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
02/18/1994
Decision Date
04/09/1996
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
RA - Radiology
Review Advisory Committee
RA - Radiology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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