K-number	K770959
Device name	BOUGIE, FILIFORM, JACKSON
Applicant	V. Mueller O.V. Baxter Healthcare Corp.
Product code	KBI
Device class	Class I
Decision date	Jun 14, 1977
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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BOUGIE, FILIFORM, JACKSON

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