K-number	K915430
Device name	SKIN STAPLE REMOVER KIT
Applicant	Cypress Medical Products, Ltd.
Product code	GDT
Device class	Class I
Decision date	Feb 28, 1992
Decision	Substantially Equivalent — Kit Device
Regulation	878.4760

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View the full FDA submission: accessdata.fda.gov

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SKIN STAPLE REMOVER KIT

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