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FDA 510(k), K072757, DIVE AND SHALLOW AND GRAND DIVE
FDA 510(k), K072757, DIVE AND SHALLOW AND GRAND DIVE
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510(K) Number: K072757
Device Name: DIVE AND SHALLOW AND GRAND DIVE
Manufacturer: SUMMIT TO SEA
Device Classification Name: chamber, hyperbaric
Regulation Number: 868.5470
Classification Product Code: CBF
Date Received: 09/27/2007
Decision Date: 02/08/2008
Regulation Medical Specialty: Anesthesiology
Device Name: DIVE AND SHALLOW AND GRAND DIVE
Manufacturer: SUMMIT TO SEA
Device Classification Name: chamber, hyperbaric
Regulation Number: 868.5470
Classification Product Code: CBF
Date Received: 09/27/2007
Decision Date: 02/08/2008
Regulation Medical Specialty: Anesthesiology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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