510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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LFFClass I

Unit, Activation, Breath Control

21 CFR 890.3920 / Physical Medicine
FDA source (opens on fda.gov)

LFF is the FDA product code for Unit, Activation, Breath Control, a class I device type, regulated under 21 CFR 890.3920. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
LFF
Device name
Unit, Activation, Breath Control
Regulation
21 CFR 890.3920
Device class
Class I
Review panel
Physical Medicine
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code LFF

By decision year
1 clearance under product code LFF with a decision year between 1998 and 1998, 1998 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code LFF by decision year
YearClearances
19981

Applicants with the most clearances

Product code LFF
Applicants holding the most 510(k) clearances under product code LFF
ApplicantClearances
Interactive Living Systems, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code