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FDA 510(k), K100268, SECHRIST MONOPLACE HYPERBARIC OXYGEN CHAMBER
FDA 510(k), K100268, SECHRIST MONOPLACE HYPERBARIC OXYGEN CHAMBER
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510(K) Number: K100268
Device Name: SECHRIST MONOPLACE HYPERBARIC OXYGEN CHAMBER
Manufacturer: SECHRIST INDUSTRIES, INC.
Device Classification Name: chamber, hyperbaric
Regulation Number: 868.5470
Classification Product Code: CBF
Date Received: 01/29/2010
Decision Date: 04/26/2010
Regulation Medical Specialty: Anesthesiology
Device Name: SECHRIST MONOPLACE HYPERBARIC OXYGEN CHAMBER
Manufacturer: SECHRIST INDUSTRIES, INC.
Device Classification Name: chamber, hyperbaric
Regulation Number: 868.5470
Classification Product Code: CBF
Date Received: 01/29/2010
Decision Date: 04/26/2010
Regulation Medical Specialty: Anesthesiology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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