K-number	K882643
Device name	AM TM SYRGICAL DRAPES
Applicant	Henley Intl.
Product code	KKX
Device class	Class II
Decision date	Mar 3, 1989
Decision	Substantially Equivalent for Some Indications
Regulation	878.4370

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View the full FDA submission: accessdata.fda.gov

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AM TM SYRGICAL DRAPES

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