K-number	K760605
Device name	LIGHTCAST II CARBIDE BLADE
Applicant	Merck, Sharp & Dohme
Product code	GES
Device class	Class I
Decision date	Oct 5, 1976
Decision	Substantially Equivalent
Regulation	878.4800

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View the full FDA submission: accessdata.fda.gov

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LIGHTCAST II CARBIDE BLADE

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