K-number	K843461
Device name	BIOGLASS OSSICULAR RECONSTRUCTION PROSTH
Applicant	American Biomaterials Corp.
Product code	ETA
Device class	Class II
Decision date	Jan 9, 1985
Decision	Substantially Equivalent
Regulation	874.3495

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View the full FDA submission: accessdata.fda.gov

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BIOGLASS OSSICULAR RECONSTRUCTION PROSTH

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