Product Code: LIH FDA class 2 21 CFR 882.5890

Interferential Current Therapy

Neurology

Interferential current therapy is a type of electrotherapy device that applies medium-frequency alternating currents that interfere with each other at the target tissue, producing a low-frequency therapeutic effect used for the relief of pain and to stimulate muscle tissue in neurological and musculoskeletal rehabilitation. The device is FDA Class 2, indicating moderate risk and requiring 510(k) premarket clearance. It carries product code LIH and is regulated under 21 CFR 882.5890 within the Neurology specialty. This device is eligible for third-party review.

510(k)s
73
FEI Numbers
46
Registration Numbers
46
Unique Applicants
50
Years Active
40

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Basic Information

Product Code
LIH
Device Class
FDA class 2
Regulation Number
882.5890
Medical Specialty
Neurology
Review Panel
NE
Submission Type
1

Device Characteristics

GMP Exempt
Implant
Life Sustain/Support
Third Party
Summary Malfunction Reporting

510(k) Clearance History

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Related 510(k) Clearances

This FDA classification is associated with 73 510(k) clearances via K numbers.

K Number Device Name
K231575 Vecttor VT-300
K202725 ETD4000
K183692 Avid IF2
K122944 GEMORE TRUE SINE INTERFERENTIAL STIMULATOR
K121662 VECTTOR VT-200
K110509 EVERYWAY INTERFERNTIAL STIMULATOR, MODEL IF-908
K100246 MAX-IF1000
K092780 INF 4160 PLUS, MODEL D-FJ31F
K092763 IF TRUE SINE INTERFERENTIAL STIMULATOR, WL-2206D
K090023 IF SERIES TRUE SINE INTERFERENTIAL STIMULATOR, MODEL: WL-2206B AND WL-2106E
K070890 EVERLIFE INTERFERENTIAL CURRENT THERAPY, MODEL IF-100507
K060975 IF TRUE SINE INTERFERENTIAL STIMULATOR / MODEL WL-2206A1 & WI-2206A2
K052289 DEEPWAVE NEUROMODULATION PAIN THERAPY DEVICE
K043407 INF 4160, MODEL D-FJ27F
K042057 INFINITY ELECTROTHERAPY SYSTEM
K040007 INTERFERENTIAL STIMULATOR, MODEL BMLS02-6
K040824 INTERFERENTIAL STIMULATOR, MODEL BMLS03-6
K032719 GM3 SERIES IF TENS, MODEL GM3X2IF (WHERE X IS A PARAMETER OF DIFFERENT HOUSING)
K033358 CHRONIC PAIN SUPPRESSOR CPS-2000, MODEL CPS-2000
K024100 IF SERIES TRUE SINE INTERFERENTIAL STIMULATOR/MODEL: WL-2206, WELL IF, LIFE IF AND THE CUSTOMER PRIVATE BRAND
K022433 NEOGENESYS 2K
K020516 CARE IFC PLUS
K013082 MEDSTAR 100 INTERFERENTIAL STIMLATOR
K003631 SMARTWAVE IF 2000
K010948 DYNATRON STS RX
K010565 DYNATRON STS
K993600 MULTI INTERFERENTIAL STIMULATOR, MODEL TR-841
K992652 SD-730 IF-SDS, PERFECT PULSE IF-SDS
K990129 TL250 INTERFERENTIAL/MUSCLE STIMULATOR INTERFERENTIAL CURRENT THERAPY MUSCLE STIMULATOR
K974585 IF-727 INTERFERENTIAL STIMULATOR
K952683 APEX MEDICAL CORP. PORTABLE INTERFERENTIAL STIMULATION DEVICE
K961261 DYNATRON 525
K955860 MULTI III, IV
K955387 ISOTRON III, ISOTRON IV
K950349 DYNATRON 950
K950348 DYNATRON 650
K941577 DYNATRON 550
K941461 DYNATRON 850
K952089 RICH-MAR CM-II COMBINED MUSCLE STIMULATOR, INTERFERENTIAL, TENS & THERAPEUTIC ULTRASOUND DEVICE
K942428 CMT-1000
K941815 ISOTRON III
K932868 THERATOUCH 4.7
K930535 IF400
K930263 MATRIX PRO-ELECDT
K931732 VIFI: VECTOR INTERFERENTIAL ONE
K931768 INTERFERENTIAL CURRENT THERAPY UNIT
K930264 MATRIX ELECDT & VACUPULLS
K925687 INTERFERENTIAL STIMULATOR MODEL IMF4150/A
K924666 INTELECT IFC2
K924961 HMP 4000 INTERFERENTIAL STIMULATOR
K924490 MASTERSTIM I-2
K924319 DYNATRON 400
K922529 POWERED MUSCLE STIMULATOR
K922020 ENDOMED 582
K915100 BRINDLEY & SMITH ET-1000
K921491 MEDI-STIM
K921954 ISOTRON III
K921953 MULTI III
K921612 INTERTRON 4500, INTERTRON 5000, MASTERSTIM I-2
K921441 INTERFERENTIAL STIMULATOR MODEL INF 4150/A
K904743 LSI SYSTEM II
K905571 ELECTRO-NERVE STIMULATOR TENS MODEL,INF 4150/A
K883896 NEUROTRAIN
K883462 IF-II (TM), MODEL 9800
K883080 SYS*STIM 220
K880924 INTER TRON 4000
K870384 ENDOMED 433
K873566 ELECTROSTIM I.F.
K874119 INTERFERENTIAL CURRENT UNIT
K861039 OMNIVAC (VACUUM ELECTRODE SYSTEM)
K854721 NEMECTRODYN MODEL 2 & ENDOVAC 2
K840321 ENDODYNE DUAL
K833305 VECTOR SEIGE 2023645 AC POWERED STIMU-

FEI Numbers

This FDA classification entry is associated with 46 FEI numbers. Click on an entry to view related FDA registrations.

Registration Numbers

This FDA classification entry is associated with 46 registration numbers. Click on an entry to view related FDA registrations.