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FDA 510(k), K011592, OXYGEN TREATMENT HOOD
FDA 510(k), K011592, OXYGEN TREATMENT HOOD
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510(K) Number: K011592
Device Name: OXYGEN TREATMENT HOOD
Manufacturer: NORMA F OCKWIG
Device Classification Name: Chamber, Hyperbaric
Regulation Number: CBF
Classification Product Code: 05/24/2001
Date Received: 06/19/2002
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Anesthesiology
Device Name: OXYGEN TREATMENT HOOD
Manufacturer: NORMA F OCKWIG
Device Classification Name: Chamber, Hyperbaric
Regulation Number: CBF
Classification Product Code: 05/24/2001
Date Received: 06/19/2002
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Anesthesiology
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- Delivery: Approximately 1 to 2 weeks
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