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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Extractor, Vacuum, Fetal
510(k) Number K890307
Device Name MITYVAC M STYLE VACUUM EXTRACTOR, DISPOSABLE
Applicant
Neward Enterprises, Inc.
P.O. Box 725
9251 Archibald Ave.
Cucamonga,  CA  91730
Applicant Contact ALLYSON C CARMACK
Correspondent
Neward Enterprises, Inc.
P.O. Box 725
9251 Archibald Ave.
Cucamonga,  CA  91730
Correspondent Contact ALLYSON C CARMACK
Regulation Number884.4340
Classification Product Code
HDB  
Date Received01/23/1989
Decision Date 03/31/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Obstetrics/Gynecology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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