K-number	K884833
Device name	ULTRA 2000 (T.E.N.S.)
Applicant	Maxima Intl., Inc.
Product code	GZJ
Device class	Class II
Decision date	Feb 13, 1989
Decision	Substantially Equivalent
Regulation	882.5890

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View the full FDA submission: accessdata.fda.gov

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ULTRA 2000 (T.E.N.S.)

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