K-number	K951181
Device name	RYDER CONTACT LENS CASE
Applicant	Bradstreet Clinical Research Assoc., Inc.
Product code	LRX
Device class	Class II
Decision date	May 12, 1995
Decision	Substantially Equivalent
Regulation	886.5928

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View the full FDA submission: accessdata.fda.gov

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RYDER CONTACT LENS CASE

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