K-number	K891123
Device name	RUBBERCARE PATIENT EXAMINATION GLOVE
Applicant	Perusahaan Pelindung Getah (M) Sdn Bhd
Product code	LYY
Device class	Class I
Decision date	Jul 14, 1989
Decision	Substantially Equivalent
Regulation	880.6250

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View the full FDA submission: accessdata.fda.gov

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RUBBERCARE PATIENT EXAMINATION GLOVE

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