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FDA 510(k), K041007, MILLENIUM, MODELS 2000, 2001 AND 2002
FDA 510(k), K041007, MILLENIUM, MODELS 2000, 2001 AND 2002
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510(K) Number: K041007
Device Name: MILLENIUM, MODELS 2000, 2001 AND 2002
Manufacturer: HYPERBARIC FOR LIFE LLC
Device Classification Name: chamber, hyperbaric
Regulation Number: 868.5470
Classification Product Code: CBF
Date Received: 04/19/2004
Decision Date: 11/15/2004
Regulation Medical Specialty: Anesthesiology
Device Name: MILLENIUM, MODELS 2000, 2001 AND 2002
Manufacturer: HYPERBARIC FOR LIFE LLC
Device Classification Name: chamber, hyperbaric
Regulation Number: 868.5470
Classification Product Code: CBF
Date Received: 04/19/2004
Decision Date: 11/15/2004
Regulation Medical Specialty: Anesthesiology
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