Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Ava Fertility Tracker

K-Number: K200163 · 2021-01-19

ApplicantAva AG
Decision Date2021-01-19
Product CodeLHD
DecisionSubstantially Equivalent

Device Summary

Ava Fertility Tracker is a medical device manufactured by Ava AG. It received FDA 510(k) clearance on 2021-01-19 under approval number K200163. The device is classified under product code LHD. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Ava Fertility Tracker?

Ava Fertility Tracker is a medical device that received FDA 510(k) clearance on 2021-01-19. It is manufactured by Ava AG. The 510(k) number is K200163.

When was Ava Fertility Tracker approved by the FDA?

Ava Fertility Tracker received FDA 510(k) clearance on 2021-01-19, under approval number K200163.

What company makes Ava Fertility Tracker?

Ava Fertility Tracker is manufactured by Ava AG.

What is the FDA product code for Ava Fertility Tracker?

The FDA product code for Ava Fertility Tracker is LHD.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.