K-number	K192324
Device name	Sheridan Spiral-Flex Endotracheal Tubes
Applicant	Teleflexmedical, Inc.
Product code	BTR
Device class	Class II
Decision date	Dec 6, 2019
Decision	Substantially Equivalent
Regulation	868.5730

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Source

View the full FDA submission: accessdata.fda.gov

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Sheridan Spiral-Flex Endotracheal Tubes

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