K-number	K811704
Device name	MULTITUBULAR AIR SPLINT KIT
Applicant	Roger Cestac & Assoc.
Product code	IQI
Device class	Class I
Decision date	Jul 1, 1981
Decision	Substantially Equivalent
Regulation	890.3475

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Source

View the full FDA submission: accessdata.fda.gov

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MULTITUBULAR AIR SPLINT KIT

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