K-number	K093696
Device name	SR GLOVE, NU GLOVE, HIGHSTRESS MODEL 801, MODEL 802, MODEL 803
Applicant	Central Medicare Sdn Bhd
Product code	LZA
Device class	Class I
Decision date	Feb 12, 2010
Decision	Substantially Equivalent
Regulation	880.6250

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View the full FDA submission: accessdata.fda.gov

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SR GLOVE, NU GLOVE, HIGHSTRESS MODEL 801, MODEL 802, MODEL 803

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