K-number	K852469
Device name	SAF-D-FIB
Applicant	Medtronic Andover Medical, Inc.
Product code	DRX
Device class	Class II
Decision date	Sep 16, 1985
Decision	Substantially Equivalent
Regulation	870.2360

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View the full FDA submission: accessdata.fda.gov

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SAF-D-FIB

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