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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name forceps, obstetrical
510(k) Number K951529
Device Name V. MUELLER OBSTETRICAL (OB) FORCEPS
Applicant
BAXTER HEALTHCARE CORP.
1500 WAUKEGAN RD.
MCGAW PK,  IL  60085
Applicant Contact NICOLE M CLARK
Correspondent
BAXTER HEALTHCARE CORP.
1500 WAUKEGAN RD.
MCGAW PK,  IL  60085
Correspondent Contact NICOLE M CLARK
Regulation Number884.4400
Classification Product Code
HDA  
Date Received04/03/1995
Decision Date 08/04/1995
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Obstetrics/Gynecology
Type Traditional
Reviewed by Third Party No
Combination Product No
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