Product code LIH— Neurology
ISOTRON III
- Classification name
- Interferential Current Therapy
- Device class
- Class 2
- Regulation
- 21 CFR 882.5890
- Advisory panel
- Neurology
- Total cleared
- 73
- First cleared
- Most recent
Market context for product code LIH
FDA has cleared devices under product code LIH between 1983 and 2024, filed by 50 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.
Clearances per year
last 15 years- 2024
- 2021
- 2019
- 2012
- 2011
- 2010
- 2009
- 2007
- 2006
- 2005
- 2004
- 2003
- 2002
- 2001
- 2000
Top applicants under product code LIH
Recent clearances under product code LIH
- 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
- K010565 — DYNATRON STS
- K010948 — DYNATRON STS RX
- 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
- K955387 — ISOTRON III, ISOTRON IV
- K955860 — MULTI III, IV
- K950348 — DYNATRON 650
- K950349 — DYNATRON 950
- K941461 — DYNATRON 850
- K941577 — DYNATRON 550
- 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
- K921953 — MULTI III
- K921954 — ISOTRON 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-
Data sourced from openFDA. This site is unofficial and independent of the FDA.