K-number	K070749
Device name	ESTECH PERCUTANEOUS INSERTION DILATOR KIT
Applicant	Coombs Medical Device Consulting
Product code	DRE
Device class	Class II
Decision date	Oct 24, 2007
Decision	Substantially Equivalent
Regulation	870.1310

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Source

View the full FDA submission: accessdata.fda.gov

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ESTECH PERCUTANEOUS INSERTION DILATOR KIT

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