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

Unit, Fluidotherapy

21 CFR 890.5100 / Physical Medicine
FDA source (opens on fda.gov)

LSB is the FDA product code for Unit, Fluidotherapy, a class II device type, regulated under 21 CFR 890.5100. As of , FDA records hold 4 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
LSB
Device name
Unit, Fluidotherapy
Regulation
21 CFR 890.5100
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
No
Ingested clearances
4
Ingested recalls
0

Clearances, product code LSB

By decision year
4 clearances under product code LSB with a decision year between 1987 and 2001, 2001 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code LSB by decision year
YearClearances
19871
19911
20012

Applicants with the most clearances

Product code LSB
Applicants holding the most 510(k) clearances under product code LSB
ApplicantClearances
Henley Intl.2
Chattanooga Group, Inc.1
Thermo-Electric Co.1

Companies listing this code with FDA

Companies whose registered establishments list this code