FEMECC ENDOCERVICAL CURETTE— 510(k) K060320

Substantially Equivalent

Femspec LLC

FDA 510(k) clearance K060320 for FEMECC ENDOCERVICAL CURETTE, Substantially Equivalent on 2006-07-28. Applicant: Femspec LLC. Device class: 2.

Clearance details

Applicant: Femspec LLC
Product code: Code PCF
Device class: Class 2
Regulation: 21 CFR 884.1050
Advisory panel: Obstetrics/Gynecology
Date received: 2006-02-08
Decision date: 2006-07-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Port Townsend, WA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.