K-number	K031248
Device name	CONSULTIVA REPORT STATION, MODEL RS-1
Applicant	Miramedica, Inc.
Product code	LLZ
Device class	Class II
Decision date	Jun 20, 2003
Decision	Substantially Equivalent
Regulation	892.2050

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View the full FDA submission: accessdata.fda.gov

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CONSULTIVA REPORT STATION, MODEL RS-1

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