iVitri Straw— 510(k) K172751

Substantially Equivalent

Reprobitech Corp.

FDA 510(k) clearance K172751 for iVitri Straw, Substantially Equivalent on 2018-02-09. Applicant: Reprobitech Corp..

Clearance details

Applicant: Reprobitech Corp.
Product code: Code MQK
Advisory panel: Obstetrics/Gynecology
Date received: 2017-09-12
Decision date: 2018-02-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Flushing, NY, US

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