K-number	K862172
Device name	QUALI-MED'S OPERATING ROOM DRAPES
Applicant	Quali-Med, Inc.
Product code	KKX
Device class	Class II
Decision date	Jun 19, 1986
Decision	Substantially Equivalent
Regulation	878.4370

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View the full FDA submission: accessdata.fda.gov

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QUALI-MED'S OPERATING ROOM DRAPES

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