FORCEPS, BIOPSY GYNECOLOGICAL INSTRU/BIOPSY— 510(k) K933767

Name: FDA 510(k) clearance K933767
Creator: U.S. Food and Drug Administration
Published: 1994-05-26

Substantially Equivalent

Mahe-Medizintechnik

FDA 510(k) clearance K933767 for FORCEPS, BIOPSY GYNECOLOGICAL INSTRU/BIOPSY, Substantially Equivalent on 1994-05-26. Applicant: Mahe-Medizintechnik. Device class: 1.

Clearance details

Applicant: Mahe-Medizintechnik
Product code: Code HFB
Device class: Class 1
Regulation: 21 CFR 884.4530
Advisory panel: Obstetrics/Gynecology
Date received: 1993-07-29
Decision date: 1994-05-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Nashville, TN, US

Download summary PDF View on FDA.gov ↗

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