K-number	K812566
Device name	UNIVERSAL SUTURE PASSER
Applicant	Ortho Pared Instruments, Inc.
Product code	GDL
Device class	Class I
Decision date	Nov 10, 1981
Decision	Substantially Equivalent
Regulation	878.4800

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View the full FDA submission: accessdata.fda.gov

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UNIVERSAL SUTURE PASSER

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