K-number	K002794
Device name	MODEL 5000 MULTIPLACE HYPERBARIC THERAPY
Applicant	Hypertec, Inc.
Product code	CBF
Device class	Class II
Decision date	Dec 6, 2000
Decision	Substantially Equivalent
Regulation	868.5470

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View the full FDA submission: accessdata.fda.gov

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MODEL 5000 MULTIPLACE HYPERBARIC THERAPY

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