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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Catheter, Percutaneous
510(k) Number K895753
Device Name BREVET DISPOSABLE CONNECTORS
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 Number870.1250
Classification Product Code
DQY  
Date Received09/26/1989
Decision Date 11/14/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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