K-number	K062480
Device name	JOYKEY SURGICAL DRAPES (STERILE)
Applicant	Joykey Industryial , Ltd.
Product code	KKX
Device class	Class II
Decision date	Mar 5, 2007
Decision	Substantially Equivalent
Regulation	878.4370

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View the full FDA submission: accessdata.fda.gov

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JOYKEY SURGICAL DRAPES (STERILE)

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