K-number	K913484
Device name	ZOLL D-900 DEFIBRILLATOR
Applicant	Zmi Corp.
Product code	LDD
Device class	Class II
Decision date	Dec 16, 1991
Decision	Substantially Equivalent
Regulation	870.5300

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View the full FDA submission: accessdata.fda.gov

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ZOLL D-900 DEFIBRILLATOR

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