K-number	K853588
Device name	FIBRELIGHT NASAL SPECULA
Applicant	Downs Surgical , Ltd.
Product code	EPY
Device class	Class I
Decision date	Dec 18, 1985
Decision	Substantially Equivalent
Regulation	878.1800

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View the full FDA submission: accessdata.fda.gov

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FIBRELIGHT NASAL SPECULA

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