K-number	K021359
Device name	DIGI-PRO TENS MODEL WL-2203 AND WL-2205
Applicant	Well-Life Healthcare, Inc.
Product code	GZJ
Device class	Class II
Decision date	Apr 30, 2002
Decision	Substantially Equivalent
Regulation	882.5890

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View the full FDA submission: accessdata.fda.gov

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DIGI-PRO TENS MODEL WL-2203 AND WL-2205

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