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

Interferential Current Therapy

21 CFR 882.5890 / Neurology
FDA source (opens on fda.gov)

LIH is the FDA product code for Interferential Current Therapy, a class II device type, regulated under 21 CFR 882.5890. As of , FDA records hold 73 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
LIH
Device name
Interferential Current Therapy
Regulation
21 CFR 882.5890
Device class
Class II
Review panel
Neurology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
73
Ingested recalls
0

Clearances, product code LIH

By decision year
73 clearances under product code LIH with a decision year between 1983 and 2024, 1992 the highest year at 8.
Show the numbers
510(k) clearances under FDA product code LIH by decision year
YearClearances
19831
19841
19862
19884
19893
19912
19928
19936
19945
19957
19963
19971
19981
19991
20001
20015
20021
20034
20043
20052
20061
20071
20092
20102
20111
20122
20191
20211
20241

Applicants with the most clearances

Product code LIH
Applicants holding the most 510(k) clearances under product code LIH
ApplicantClearances
Dynatronics Corp.7
BioMedical Life Systems Inc.5
Excel Tech., Ltd.5
FUJI Dynamics Limited2
Gemore Technology Co., Ltd.2
Henley Intl.2
Matrix Electromedical, Inc.2
Rich-Mar Corp.2
Skylark Device Co., Ltd.2
Theratech, Inc.2

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 45 companies shown, in name order