K-number	K760051
Device name	TRAY, SUTURE REMOVAL
Applicant	M-C Ind., Inc.
Product code	KDD
Device class	Class I
Decision date	Aug 30, 1976
Decision	Substantially Equivalent
Regulation	878.4800

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View the full FDA submission: accessdata.fda.gov

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TRAY, SUTURE REMOVAL

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