FEMTEST ENDOMETRIAL SUCTION CURETTE, MODEL FT-1— 510(k) K051294

Name: FDA 510(k) clearance K051294
Creator: U.S. Food and Drug Administration
Published: 2005-12-21

Substantially Equivalent

Femspec LLC

FDA 510(k) clearance K051294 for FEMTEST ENDOMETRIAL SUCTION CURETTE, MODEL FT-1, Substantially Equivalent on 2005-12-21. Applicant: Femspec LLC. Device class: 2.

Clearance details

Applicant: Femspec LLC
Product code: Code HHK
Device class: Class 2
Regulation: 21 CFR 884.1175
Advisory panel: Obstetrics/Gynecology
Date received: 2005-05-18
Decision date: 2005-12-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Port Townsend, WA, US

Download summary PDF View on FDA.gov ↗

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