K-number	K892005
Device name	SHOCK ADVISORY ADAPTER FOR USE W/LIFEPAK 9
Applicant	Physio-Control Corp.
Product code	MKJ
Device class	Class III
Decision date	Jun 20, 1989
Decision	Substantially Equivalent
Regulation	870.5310

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View the full FDA submission: accessdata.fda.gov

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SHOCK ADVISORY ADAPTER FOR USE W/LIFEPAK 9

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