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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name arthroscope
510(k) Number K943985
Device Name LIMITED REUSE BLADES
Applicant
LINVATEC CORP.
11311 CONCEPT BLVD.
LARGO,  FL  33773
Applicant Contact CAROL A WEIDEMAN
Correspondent
LINVATEC CORP.
11311 CONCEPT BLVD.
LARGO,  FL  33773
Correspondent Contact CAROL A WEIDEMAN
Regulation Number888.1100
Classification Product Code
HRX  
Subsequent Product Code
HWE  
Date Received08/16/1994
Decision Date 11/07/1994
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Type Traditional
Reviewed by Third Party No
Combination Product No
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