Product code LFF— Physical Medicine

IVOC- INTEGRATED VOICE OPERATED CONTROL UNIT (IVOC-1)

Classification name
Unit, Activation, Breath Control
Device class
Class 1
Regulation
21 CFR 890.3920
Advisory panel
Physical Medicine
Total cleared
1
First cleared
Most recent

Market context for product code LFF

FDA has cleared 1 device under product code LFF, all in 1998, filed by 1 applicant company. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

Top applicants under product code LFF

Recent clearances under product code LFF

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