K-number	K210509
Device name	Rocket Platinum Cured Cathter
Applicant	Rocket Medical Plc
Product code	DWM
Device class	Class II
Decision date	Sep 9, 2021
Decision	Unknown
Regulation	870.5050

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Source

View the full FDA submission: accessdata.fda.gov

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Rocket Platinum Cured Cathter

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