K-number	K090183
Device name	HERCULES 3 STAGE WIRE GUIDED DILATION BALLOON
Applicant	Cook Endoscopy
Product code	KNQ
Device class	Class II
Decision date	Sep 25, 2009
Decision	Substantially Equivalent
Regulation	876.5365

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Source

View the full FDA submission: accessdata.fda.gov

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HERCULES 3 STAGE WIRE GUIDED DILATION BALLOON

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