K-number	K962389
Device name	EUROMEDICAL REINFORCED ENDOTRACHEAL TUBE
Applicant	Unomedical Sdn Bhd
Product code	BTR
Device class	Class II
Decision date	Nov 21, 1996
Decision	Substantially Equivalent
Regulation	868.5730

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View the full FDA submission: accessdata.fda.gov

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EUROMEDICAL REINFORCED ENDOTRACHEAL TUBE

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