K-number	K895767
Device name	ORIGINAL TICK KIT/1ST AID KIT
Applicant	Tick Kit, Inc.
Product code	LRR
Device class	Class N
Decision date	Dec 22, 1989
Decision	Substantially Equivalent — Same Device
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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ORIGINAL TICK KIT/1ST AID KIT

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