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FDA 510(k), K800023, LUNG AEROSOL UNIT
FDA 510(k), K800023, LUNG AEROSOL UNIT
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$49.00 USD
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$49.00 USD
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510(K) Number: K800023
Device Name: LUNG AEROSOL UNIT
Manufacturer:
Device Classification Name: Nebulizer (Direct Patient Interface)
Regulation Number: CAF
Classification Product Code: KXA
Date Received: 01/07/1980
Decision Date: 01/01/1985
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
Device Name: LUNG AEROSOL UNIT
Manufacturer:
Device Classification Name: Nebulizer (Direct Patient Interface)
Regulation Number: CAF
Classification Product Code: KXA
Date Received: 01/07/1980
Decision Date: 01/01/1985
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
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