K-number	K971359
Device name	RESTORE (A.K.A. CAPSURE)
Applicant	Nebl, Inc.
Product code	MNG
Device class	Class I
Decision date	Nov 14, 1997
Decision	Substantially Equivalent
Regulation	876.5160

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View the full FDA submission: accessdata.fda.gov

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RESTORE (A.K.A. CAPSURE)

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