K-number	K000906
Device name	KLINIDRAPE SURGICAL DRAPES
Applicant	Molnlycke Health Care, Inc.
Product code	KKX
Device class	Class II
Decision date	Jun 23, 2000
Decision	Substantially Equivalent
Regulation	878.4370

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View the full FDA submission: accessdata.fda.gov

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KLINIDRAPE SURGICAL DRAPES

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