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FDA 510(k) Application Details - K993359
Device Classification Name
Accelerator, Linear, Medical
More FDA Info for this Device
510(K) Number
K993359
Device Name
Accelerator, Linear, Medical
Applicant
NOMOS CORP.
2591 WEXFORD BAYNE RD.
SUITE 400
SEWICKLEY, PA 15143 US
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Contact
WILLIAM O CHISHKO
Other 510(k) Applications for this Contact
Regulation Number
892.5050
More FDA Info for this Regulation Number
Classification Product Code
IYE
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More FDA Info for this Product Code
Date Received
10/06/1999
Decision Date
12/21/1999
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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