K-number	K781418
Device name	XOMED TRANSSPHENOIDAL HANDPIECE
Applicant	Xomed, Inc.
Product code	ERL
Device class	Class II
Decision date	Aug 31, 1978
Decision	Substantially Equivalent
Regulation	874.4250

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View the full FDA submission: accessdata.fda.gov

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XOMED TRANSSPHENOIDAL HANDPIECE

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