So why would FDA be reclassifying electrocardiograph software into over-the-counter?
(www.federalregister.gov)
You're viewing a single comment thread. View all comments, or full comment thread.
Comments (3)
sorted by:
The reclassification is on track to permit Apple and other vendors capability to use those "hear beat monitor" aps to print out results or transmit to somebody for the readings to be analyzed. Follow the Benjamins, Baby! Oy Vey!
Yes and with many more vax induced heart conditions to monitor = Ka ching $$