K-number	K820451
Device name	INTRODUCER FOR ENDOTRACHEAL TUBE
Applicant	Imed Corp.
Product code	BWB
Device class	Class I
Decision date	Mar 26, 1982
Decision	Substantially Equivalent
Regulation	868.5780

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View the full FDA submission: accessdata.fda.gov

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INTRODUCER FOR ENDOTRACHEAL TUBE

Everything you need for a 510(k) submission. Nothing you don't.