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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Accelerator, Linear, Medical
510(k) Number K963258
Device Name PEACOCK SYSTEM
Applicant
Nomos Corp.
2591 Wexford Bayne Rd.
Suite 400
Sewickley,  PA  15143
Applicant Contact MARVIN L SUSSAMN, PH.D.
Correspondent
Nomos Corp.
2591 Wexford Bayne Rd.
Suite 400
Sewickley,  PA  15143
Correspondent Contact MARVIN L SUSSAMN, PH.D.
Regulation Number892.5050
Classification Product Code
IYE  
Date Received08/20/1996
Decision Date 11/18/1996
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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