Ava Fertility Tracker— 510(k) K200163

Substantially Equivalent

Ava AG

FDA 510(k) clearance K200163 for Ava Fertility Tracker, Substantially Equivalent on 2021-01-19. Applicant: Ava AG. Device class: Unclassified.

Clearance details

Applicant: Ava AG
Product code: Code LHD
Device class: Unclassified
Advisory panel: Unknown
Date received: 2020-01-22
Decision date: 2021-01-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Zurich, CH

Download summary PDF View on FDA.gov ↗

Recent devices under product code LHD

K122337 — OVUSENSE2013-08-06
K102499 — DUOFERTILITY2011-12-20
K050094 — LADY COMP USA2006-04-20
K030961 — MICROLIFE DIGITAL BASAL THERMOMETER, MODEL MT 19212003-09-12
K021978 — PETIT SOPHIA2003-04-08

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