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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Instrument, Ultrasonic Surgical
510(k) Number K933559
Device Name ALLIGER ULTRASONIC SURGICAL SYSTEM
Applicant
MEDSONIC, INC.
1938 NEW HIGHWAY
FARMINGDALE,  NY  11735
Applicant Contact VALERIE ALLIGER
Correspondent
MEDSONIC, INC.
1938 NEW HIGHWAY
FARMINGDALE,  NY  11735
Correspondent Contact VALERIE ALLIGER
Classification Product Code
LFL  
Date Received07/22/1993
Decision Date 10/15/1993
Decision Substantially Equivalent (SESE)
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
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