K-number	K980436
Device name	CLASS III REVERSE PULL FACEMASK
Applicant	Ortho Kinetics Corp.
Product code	DZB
Device class	Class II
Decision date	Apr 27, 1998
Decision	Substantially Equivalent
Regulation	872.5500

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View the full FDA submission: accessdata.fda.gov

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CLASS III REVERSE PULL FACEMASK

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