K-number	K911756
Device name	POSTERIOR NASAL EPISTAXIS INSTRUMENTS
Applicant	Richard Wolf Medical Instruments Corp.
Product code	ECB
Device class	Class I
Decision date	Oct 24, 1991
Decision	Substantially Equivalent
Regulation	872.4565

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View the full FDA submission: accessdata.fda.gov

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POSTERIOR NASAL EPISTAXIS INSTRUMENTS

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