K-number	K845046
Device name	PUL,MONARY ARTERY VENT CATHETER
Applicant	Dlp, Inc.
Product code	DWF
Device class	Class II
Decision date	Apr 3, 1985
Decision	Substantially Equivalent
Regulation	870.4210

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View the full FDA submission: accessdata.fda.gov

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PUL,MONARY ARTERY VENT CATHETER

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