K-number	K822220
Device name	COOPER VISION I/A SYSTEM III MODEL 1500
Applicant	CooperVision, Inc.
Product code	HQE
Device class	Class II
Decision date	Oct 6, 1982
Decision	Substantially Equivalent
Regulation	886.4150

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View the full FDA submission: accessdata.fda.gov

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COOPER VISION I/A SYSTEM III MODEL 1500

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