K-number	K811577
Device name	CROUCH CORNEAL PROTECTOR
Applicant	Denver Biomedicals, Inc.
Product code	HOY
Device class	Class I
Decision date	Aug 7, 1981
Decision	Substantially Equivalent
Regulation	886.4750

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Source

View the full FDA submission: accessdata.fda.gov

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CROUCH CORNEAL PROTECTOR

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