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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name light, surgical, fiberoptic
510(k) Number K870942
Device Name MVS FIBEROPTIC LIGHTPIPE
Applicant
ADVANCED SURGICAL PRODUCTS, INC.
524 CHELE DRIVE ST.
CHARLES,  MO  63303
Applicant Contact TODD HESSEL
Correspondent
ADVANCED SURGICAL PRODUCTS, INC.
524 CHELE DRIVE ST.
CHARLES,  MO  63303
Correspondent Contact TODD HESSEL
Regulation Number878.4580
Classification Product Code
FST  
Date Received03/09/1987
Decision Date 04/03/1987
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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