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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name goniometer, nonpowered
510(k) Number K901744
Device Name DOBBHOFF(R) RETRIEVAL FORCEPS
Applicant
BIOSEARCH MEDICAL PRODUCTS, INC.
35 INDUSTRIAL PKWY.
P.O. BOX 1700
SOMERVILLE,  NJ  08876
Applicant Contact PETER WAEGER
Correspondent
BIOSEARCH MEDICAL PRODUCTS, INC.
35 INDUSTRIAL PKWY.
P.O. BOX 1700
SOMERVILLE,  NJ  08876
Correspondent Contact PETER WAEGER
Regulation Number888.1520
Classification Product Code
KQW  
Date Received04/17/1990
Decision Date 07/03/1990
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
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