K-number	K811627
Device name	ARROW PERITONEAL LAVAGE CATHERIZATION K
Applicant	Arrow Intl., Inc.
Product code	GBW
Device class	Class I
Decision date	Aug 10, 1981
Decision	Substantially Equivalent
Regulation	878.4200

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View the full FDA submission: accessdata.fda.gov

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ARROW PERITONEAL LAVAGE CATHERIZATION K

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