K-number	K902687
Device name	STERI-CATH-DL
Applicant	Concord/Portex
Product code	BSY
Device class	Class I
Decision date	Aug 29, 1990
Decision	Substantially Equivalent
Regulation	868.6810

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View the full FDA submission: accessdata.fda.gov

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STERI-CATH-DL

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