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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Forceps, Biopsy, Gynecological
510(k) Number K933767
Device Name FORCEPS, BIOPSY GYNECOLOGICAL INSTRU/BIOPSY
Applicant
Mahe-Medizintechnik
300 James Robertson Pkwy.
Nashville,  TN  37201
Applicant Contact WINFRIED REICH
Correspondent
Mahe-Medizintechnik
300 James Robertson Pkwy.
Nashville,  TN  37201
Correspondent Contact WINFRIED REICH
Regulation Number884.4530
Classification Product Code
HFB  
Date Received07/29/1993
Decision Date 05/26/1994
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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