INTRAUTERINE INSEMINATION (IUI) CATHETER— 510(k) K092579

Substantially Equivalent

Fertiligent, Ltd.

FDA 510(k) clearance K092579 for INTRAUTERINE INSEMINATION (IUI) CATHETER, Substantially Equivalent on 2010-04-02. Applicant: Fertiligent, Ltd..

Clearance details

Applicant: Fertiligent, Ltd.
Product code: Code MQF
Advisory panel: Obstetrics/Gynecology
Date received: 2009-08-17
Decision date: 2010-04-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Indianapolis, IN, US

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