Alivecor SFO

FDA Regulatory Profile

Alivecor SFO appears in FDA public data with 1 recall, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-1125-2015, Class III) was initiated on January 9, 2015.

Summary

Total Recalls
1
510(k) Clearances
0
Inspections
0
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-1125-2015Class IIIAlive ECG App 2.1.2 ( a medical device application for the Apple iOS operating system, intended to bJanuary 9, 2015