K-number	K072379
Device name	MPS OXIPORT AND MPS OXIPORT PLUS
Applicant	Innerspace, Inc.
Product code	GWM
Device class	Class II
Decision date	Apr 29, 2008
Decision	Substantially Equivalent
Regulation	882.1620

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View the full FDA submission: accessdata.fda.gov

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MPS OXIPORT AND MPS OXIPORT PLUS

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