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

Device, Fluidized Therapy, Dry Heat

21 CFR 890.5500 / Physical Medicine
FDA source (opens on fda.gov)

LBG is the FDA product code for Device, Fluidized Therapy, Dry Heat, a class II device type, regulated under 21 CFR 890.5500. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
LBG
Device name
Device, Fluidized Therapy, Dry Heat
Regulation
21 CFR 890.5500
Device class
Class II
Review panel
Physical Medicine
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
1
Ingested recalls
0

Clearances, product code LBG

By decision year
1 clearance under product code LBG with a decision year between 1984 and 1984, 1984 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code LBG by decision year
YearClearances
19841

Applicants with the most clearances

Product code LBG
Applicants holding the most 510(k) clearances under product code LBG
ApplicantClearances
Electronic Energy, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code LBG.