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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 K940663
Device Name PEACOCK PLAN
Applicant
Nomos Corp.
2593 Wexford Bayne Rd.
Suite 315
Sewickley,  PA  15143
Applicant Contact HARRIS S TARGOVNIK, PH.D.
Correspondent
Nomos Corp.
2593 Wexford Bayne Rd.
Suite 315
Sewickley,  PA  15143
Correspondent Contact HARRIS S TARGOVNIK, PH.D.
Regulation Number892.5050
Classification Product Code
IYE  
Date Received02/18/1994
Decision Date 04/09/1996
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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