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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Perimeter, Automatic, Ac-Powered
510(k) Number K852936
Device Name THE FIELDMASTER MODEL 275
Applicant
SYNEMED, INC.
1215 FOURTH ST.
BERKELEY,  CA  94710
Applicant Contact DOUGLAS DONALDSON
Correspondent
SYNEMED, INC.
1215 FOURTH ST.
BERKELEY,  CA  94710
Correspondent Contact DOUGLAS DONALDSON
Regulation Number886.1605
Classification Product Code
HPT  
Date Received07/10/1985
Decision Date 10/15/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ophthalmic
510k Review Panel Ophthalmic
Type Traditional
Reviewed by Third Party No
Combination Product No
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