K-number	K951644
Device name	ACUTEK'S CLEARPASSAGE
Applicant	Acutek Adhesive Specialties, Inc.
Product code	LWF
Device class	Class I
Decision date	Jul 3, 1995
Decision	Substantially Equivalent
Regulation	874.3900

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View the full FDA submission: accessdata.fda.gov

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ACUTEK'S CLEARPASSAGE

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