K-number	K926045
Device name	SKYTRON LIFE ISLAND 21
Applicant	Skytron, Div. the Kmw Group, Inc.
Product code	FNM
Device class	Class II
Decision date	Jul 27, 1993
Decision	Substantially Equivalent
Regulation	880.5550

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View the full FDA submission: accessdata.fda.gov

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SKYTRON LIFE ISLAND 21

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