WALLACH FLEXIBLE ENDOMETRIAL SAMPLER— 510(k) K902693

Name: FDA 510(k) clearance K902693
Creator: U.S. Food and Drug Administration
Published: 1991-01-31

Substantially Equivalent

Wallach Surgical Devices, Inc.

FDA 510(k) clearance K902693 for WALLACH FLEXIBLE ENDOMETRIAL SAMPLER, Substantially Equivalent on 1991-01-31. Applicant: Wallach Surgical Devices, Inc.. Device class: 2.

Clearance details

Applicant: Wallach Surgical Devices, Inc.
Product code: Code HFF
Device class: Class 2
Regulation: 21 CFR 884.1060
Advisory panel: Obstetrics/Gynecology
Date received: 1990-06-19
Decision date: 1991-01-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Milford, CT, US

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