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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name powered laser surgical instrument
510(k) Number K911457
Device Name TRIMEDYNE MODEL 1210 OMNIPULSE HOLMIUM LASER SYST
Applicant
TRIMEDYNE, INC.
2801 BARRANCA RD.
IRVINE,  CA  92714 -5114
Applicant Contact MERRITT GIRGIS
Correspondent
TRIMEDYNE, INC.
2801 BARRANCA RD.
IRVINE,  CA  92714 -5114
Correspondent Contact MERRITT GIRGIS
Regulation Number878.4810
Classification Product Code
GEX  
Date Received04/03/1991
Decision Date 09/05/1991
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
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