K-number	K020314
Device name	DIGI-PRO TENS, MODEL WL-2204 AND WL-2205
Applicant	Well-Life Healthcare, Inc.
Product code	IPF
Device class	Class II
Decision date	Apr 30, 2002
Decision	Substantially Equivalent
Regulation	890.5850

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View the full FDA submission: accessdata.fda.gov

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DIGI-PRO TENS, MODEL WL-2204 AND WL-2205

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