K-number	K913230
Device name	UNIDIRECTIONAL OCCLUDER
Applicant	Welch Allyn, Inc.
Product code	HOY
Device class	Class I
Decision date	Oct 2, 1991
Decision	Substantially Equivalent
Regulation	886.4750

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View the full FDA submission: accessdata.fda.gov

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UNIDIRECTIONAL OCCLUDER

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