K-number	K971064
Device name	BAYERS BIMANUAL I/A HANDPIECES
Applicant	Visioncare Devices, Inc.
Product code	HQC
Device class	Class II
Decision date	Jun 9, 1997
Decision	Substantially Equivalent
Regulation	886.4670

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View the full FDA submission: accessdata.fda.gov

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BAYERS BIMANUAL I/A HANDPIECES

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