510(k) K053285

Device
MAGBODY DT-1200, DT-1200T, DT-1200M, DT-1200PT, DT-1200PM
Applicant
DURTECH SYSTEM CORP.
510(k) number
K053285
Product code
IPF  
Decision
Substantially Equivalent (SESE)
Decision date
2006-01-05
Date received
2005-11-25
Regulation
890.5850
Classification name
Stimulator, Muscle, Powered
Medical specialty
Physical Medicine
Review panel
Physical Medicine
Device class
2
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
Yes

Applicant Contact#

Contact
ADA LIN
Address
3f, # 27, Ln. 381 Fu-The 1st Rd. His-Chih Taipei TW 221 221

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

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Legacy Summary#

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FDA Review#

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