K-number	K935922
Device name	360 SLX ADVISORY DEFIBRILLATOR
Applicant	Medical Research Laboratories, Inc.
Product code	MKJ
Device class	Class III
Decision date	Dec 22, 1994
Decision	Substantially Equivalent
Regulation	870.5310

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View the full FDA submission: accessdata.fda.gov

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360 SLX ADVISORY DEFIBRILLATOR

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