FDA 510(k), K200163, Ava Fertility Tracker

FDA 510(k), K200163, Ava Fertility Tracker

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510(K) Number: K200163
Device Name: Ava Fertility Tracker
Manufacturer: Ava AG
Device Classification Name: device, fertility diagnostic, proceptive
Regulation Number:
Classification Product Code: LHD
Date Received: 01/22/2020
Decision Date: 01/19/2021
Regulation Medical Specialty:

NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.

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