K-number	K871546
Device name	SAFESIDE(TM) LUMED
Applicant	Luther Medical Products, Inc.
Product code	FOZ
Device class	Class II
Decision date	Jun 17, 1987
Decision	Substantially Equivalent
Regulation	880.5200

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View the full FDA submission: accessdata.fda.gov

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SAFESIDE(TM) LUMED

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