K-number	K911632
Device name	CAPIOX(R) BUBBLE TRAP
Applicant	Terumo Medical Corp.
Product code	KRL
Device class	Class II
Decision date	Jul 9, 1991
Decision	Substantially Equivalent
Regulation	870.4205

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View the full FDA submission: accessdata.fda.gov

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CAPIOX(R) BUBBLE TRAP

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