K-number	K895781
Device name	ANSELL E.P. EXTRA-PROTECTION EXAMINATION GLOVES
Applicant	Ansell Intl.
Product code	LZC
Device class	Class I
Decision date	Mar 9, 1990
Decision	Substantially Equivalent
Regulation	880.6250

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View the full FDA submission: accessdata.fda.gov

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ANSELL E.P. EXTRA-PROTECTION EXAMINATION GLOVES

Everything you need for a 510(k) submission. Nothing you don't.