K-number	K902282
Device name	ULTRA.SPEC NON-STERILE LATEX EXAMINATION GLOVE
Applicant	Ncl Corp.
Product code	LYY
Device class	Class I
Decision date	Jun 7, 1990
Decision	Substantially Equivalent
Regulation	880.6250

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View the full FDA submission: accessdata.fda.gov

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ULTRA.SPEC NON-STERILE LATEX EXAMINATION GLOVE

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