K-number	K895132
Device name	CONNELL-STEPHENS ENDO ANESS TUBE
Applicant	The Traumafuse Co.
Product code	BTR
Device class	Class II
Decision date	Oct 13, 1989
Decision	Substantially Equivalent
Regulation	868.5730

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View the full FDA submission: accessdata.fda.gov

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CONNELL-STEPHENS ENDO ANESS TUBE

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