K-number	K923830
Device name	XOMED-TREACE ALPHASCOPE
Applicant	Xomed-Treace, Inc.
Product code	ERA
Device class	Class I
Decision date	Nov 9, 1992
Decision	Substantially Equivalent
Regulation	874.4770

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View the full FDA submission: accessdata.fda.gov

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XOMED-TREACE ALPHASCOPE

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