K-number	K851613
Device name	CENTRIMED SYSTEM 1 W/SYSTEM 1 ADAPTER
Applicant	Centrimed Corp.
Product code	KFM
Device class	Class II
Decision date	Jun 19, 1985
Decision	Substantially Equivalent
Regulation	870.4360

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View the full FDA submission: accessdata.fda.gov

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CENTRIMED SYSTEM 1 W/SYSTEM 1 ADAPTER

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