K-number	K901749
Device name	TABA PATIENT EXAMINATION GLOVES
Applicant	R.S.T. Corp.
Product code	LYY
Device class	Class I
Decision date	May 30, 1990
Decision	Substantially Equivalent
Regulation	880.6250

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View the full FDA submission: accessdata.fda.gov

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TABA PATIENT EXAMINATION GLOVES

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