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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name tray, surgical, instrument
510(k) Number K882617
Device Name BREVET CASSETTE STERILIZATION MODULE
Applicant
BREVET, INC.
3630 MIRALOMA
P.O. BOX 17713
ANAHEM,  CA  92806
Applicant Contact TIMOTHY DIAMOND
Correspondent
BREVET, INC.
3630 MIRALOMA
P.O. BOX 17713
ANAHEM,  CA  92806
Correspondent Contact TIMOTHY DIAMOND
Regulation Number878.4800
Classification Product Code
FSM  
Date Received06/24/1988
Decision Date 07/28/1988
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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