K-number	K895752
Device name	DIAMOND BLADE SURGICAL KNIVES
Applicant	Magnum Diamond, Inc.
Product code	GDM
Device class	Class I
Decision date	Oct 17, 1989
Decision	Substantially Equivalent
Regulation	878.4800

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View the full FDA submission: accessdata.fda.gov

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DIAMOND BLADE SURGICAL KNIVES

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