K-number	K852491
Device name	AMERICAN PHARMASEAL TRIPLE LUMEN CATHETER
Applicant	American Pharmaseal Div. Ahsc
Product code	DQY
Device class	Class II
Decision date	Sep 25, 1985
Decision	Substantially Equivalent
Regulation	870.1250

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View the full FDA submission: accessdata.fda.gov

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AMERICAN PHARMASEAL TRIPLE LUMEN CATHETER

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