K-number	K935817
Device name	MEDSIM 300 PATIENT SIMULATOR
Applicant	Dynatech/Nevada, Inc.
Product code	DRT
Device class	Class II
Decision date	Jan 18, 1994
Decision	Substantially Equivalent
Regulation	870.2300

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View the full FDA submission: accessdata.fda.gov

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MEDSIM 300 PATIENT SIMULATOR

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