Product code LHD— Unknown
Ava Fertility Tracker
- Classification name
- Device, Fertility Diagnostic, Proceptive
- Device class
- Unclassified
- Advisory panel
- Unknown
- Total cleared
- 24
- First cleared
- Most recent
Market context for product code LHD
FDA has cleared devices under product code LHD between 1981 and 2021, filed by 21 applicant companies. No FDA device recalls reference this product code.
Clearances per year
last 15 years- 2021
- 2013
- 2011
- 2006
- 2003
- 2001
- 1995
- 1992
- 1990
- 1988
- 1987
- 1985
- 1984
- 1983
- 1982
Top applicants under product code LHD
Recent clearances under product code LHD
- K200163 — Ava Fertility Tracker
- K122337 — OVUSENSE
- K102499 — DUOFERTILITY
- K050094 — LADY COMP USA
- K030961 — MICROLIFE DIGITAL BASAL THERMOMETER, MODEL MT 1921
- K021978 — PETIT SOPHIA
- K002726 — TCOYF FERTILITY SOFTWARE VERSION 1.0
- K952756 — MEDI-AID BASAL THERMOMETER
- K945427 — B-D DIGITAL THERMOMETER
- K904211 — BIOSELF 2000 FERTILITY INDICATOR
- K901512 — L SOPHIA
- K880618 — FERTILITY FORECASTER COMPUTER PROGRAM
- K870999 — GENDER CHOICE INFORMATION KIT, FEMALE AND MALE
- K870528 — OVU-TRAC OVULATION TIMING KIT
- K852194 — MODEL MT-50 DIGITAL MEMORY FEVER & BASAL THERMOMET
- K852801 — BIOCHRON FERTILITY INDICATOR
- K845009 — RABBIT-PERSONAL COMPUTER FOR WOMEN
- K844043 — OVUDATE
- K843699 — BIOSELF TM 110
- K823463 — RIGHT TIME RHYTHM CLOCK
- K823209 — BIOSELF 101
- K821507 — SYMPTOTHERM 8 FERTILITY INDICATOR
- K813497 — RHYTHM WHEEL
- K810832 — FORECASTER
Data sourced from openFDA. This site is unofficial and independent of the FDA.