K-number	K992439
Device name	NORODYN 8000 SEMG SYSTEM, ND-8000
Applicant	Myotronics-Noromed, Inc.
Product code	HCC
Device class	Class II
Decision date	Aug 13, 1999
Decision	Substantially Equivalent
Regulation	882.5050

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View the full FDA submission: accessdata.fda.gov

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NORODYN 8000 SEMG SYSTEM, ND-8000

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