K-number	K872468
Device name	JOVI MYELOGRAPHY HARNESS
Applicant	Jovi, Inc.
Product code	KPR
Device class	Class II
Decision date	Jul 1, 1987
Decision	Substantially Equivalent
Regulation	892.1680

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View the full FDA submission: accessdata.fda.gov

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JOVI MYELOGRAPHY HARNESS

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