K-number	K871073
Device name	OMEGA BIVALVE NASAL SPLINTS
Applicant	Omega Silicone, Inc.
Product code	FYI
Device class	Class I
Decision date	May 11, 1987
Decision	Substantially Equivalent
Regulation	878.3250

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View the full FDA submission: accessdata.fda.gov

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OMEGA BIVALVE NASAL SPLINTS

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