FDA.reportPublic FDA data

510(k) K024100

Device
IF SERIES TRUE SINE INTERFERENTIAL STIMULATOR/MODEL: WL-2206, WELL IF, LIFE IF AND THE CUSTOMER PRIVATE BRAND
Applicant
Theratech, Inc.
510(k) number
K024100
Product code
LIH
Decision
Substantially Equivalent (SESE)
Decision date
2003-02-25
Date received
2002-12-12
Regulation
882.5890
Classification name
Interferential Current Therapy
Medical specialty
Neurology
Review panel
Neurology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Applicant Contact#

Contact
TONY C.S. CHANG
Address
#5,Aly. 5,Lang Cheng Hsing, Chung Ching Rd.,Pei Tun Dist. Taichung TW R.O.C R.O.C

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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K070890EVERLIFE INTERFERENTIAL CURRENT THERAPY, MODEL IF-100507Everlife Medical Equipment Co., Ltd.2007-06-29
K060975IF TRUE SINE INTERFERENTIAL STIMULATOR / MODEL WL-2206A1 & WI-2206A2Theratech, Inc.2006-05-10
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K043407INF 4160, MODEL D-FJ27FFuji Dynamics Limited2005-02-11
K042057INFINITY ELECTROTHERAPY SYSTEMEmpi2004-12-17