K-number	K900054
Device name	KESTREL LENS CASE 1543-893S/P-1700-2611
Applicant	Kestrel
Product code	LRX
Device class	Class II
Decision date	Jan 30, 1990
Decision	Substantially Equivalent
Regulation	886.5928

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View the full FDA submission: accessdata.fda.gov

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KESTREL LENS CASE 1543-893S/P-1700-2611

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