FDA 510(k), K090244, SWIFT FX
FDA 510(k), K090244, SWIFT FX
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510(K) Number: K090244
Device Name: SWIFT FX
Manufacturer:
Device Classification Name: Ventilator, Non-Continuous (Respirator)
Regulation Number: 868.5905
Classification Product Code: BZD
Date Received: 02/02/2009
Decision Date: 04/13/2009
Regulation Medical Specialty: Anesthesiology
Device Name: SWIFT FX
Manufacturer:
Device Classification Name: Ventilator, Non-Continuous (Respirator)
Regulation Number: 868.5905
Classification Product Code: BZD
Date Received: 02/02/2009
Decision Date: 04/13/2009
Regulation Medical Specialty: Anesthesiology