K-number	K922270
Device name	PHYSIOTECH 4000 OR NORODYN 8000
Applicant	Myo-Tronics, Inc.
Product code	HCC
Device class	Class II
Decision date	Sep 2, 1994
Decision	Substantially Equivalent
Regulation	882.5050

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View the full FDA submission: accessdata.fda.gov

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PHYSIOTECH 4000 OR NORODYN 8000

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