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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name laser, ophthalmic
510(k) Number K893709
Device Name COHERENT MARIE ARGON PHOTOCOAGULATOR
Applicant
COHERENT MEDICAL GROUP
3270 W. BAYSHORE RD.
P.O. BOX 10122
PALO ALTO,  CA  94303
Applicant Contact VIRGINIA SINGER
Correspondent
COHERENT MEDICAL GROUP
3270 W. BAYSHORE RD.
P.O. BOX 10122
PALO ALTO,  CA  94303
Correspondent Contact VIRGINIA SINGER
Regulation Number886.4390
Classification Product Code
HQF  
Date Received05/18/1989
Decision Date 06/15/1989
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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