K-number	K080304
Device name	PRO TENS, MODEL WL-240 RX
Applicant	Well-Life Healthcare Limited
Product code	GZJ
Device class	Class II
Decision date	Jun 20, 2008
Decision	Substantially Equivalent
Regulation	882.5890

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View the full FDA submission: accessdata.fda.gov

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PRO TENS, MODEL WL-240 RX

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