K-number	K983164
Device name	RESTORE (AKA RE/STOR)
Applicant	Nebl, Inc.
Product code	MNG
Device class	Class I
Decision date	Mar 5, 1999
Decision	Substantially Equivalent
Regulation	876.5160

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Source

View the full FDA submission: accessdata.fda.gov

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RESTORE (AKA RE/STOR)

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