K-number	K820104
Device name	NUPRO* GEL TRAY
Applicant	Johnson & Johnson Professionals, Inc.
Product code	KMT
Device class	Class I
Decision date	Feb 23, 1982
Decision	Substantially Equivalent
Regulation	872.6870

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View the full FDA submission: accessdata.fda.gov

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NUPRO* GEL TRAY

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