K-number	K012362
Device name	MODIFICATION TO VASCULAR CLOSURE DEVICE
Applicant	Std Mfg., Inc.
Product code	GDW
Device class	Class II
Decision date	Aug 23, 2001
Decision	Substantially Equivalent
Regulation	878.4750

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO VASCULAR CLOSURE DEVICE

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