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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name forceps, ophthalmic
510(k) Number K851791
Device Name 37-610 TO 37-880 VARIOUS OPHTHAL-FORCEPS
Applicant
ARTIBERIA
4518 LOS RANCHITOS
SAN ANTONIO,  TX  78233
Applicant Contact GIL M SANCHEZ
Correspondent
ARTIBERIA
4518 LOS RANCHITOS
SAN ANTONIO,  TX  78233
Correspondent Contact GIL M SANCHEZ
Regulation Number886.4350
Classification Product Code
HNR  
Date Received04/25/1985
Decision Date 05/30/1985
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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