K-number	K911604
Device name	MDPHONE CELLULAR + RESCUE (DEFIB SYSTEM)
Applicant	Medphone Corp.
Product code	LDD
Device class	Class II
Decision date	Sep 23, 1991
Decision	Substantially Equivalent
Regulation	870.5300

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View the full FDA submission: accessdata.fda.gov

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MDPHONE CELLULAR + RESCUE (DEFIB SYSTEM)

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