FDA 510(k), K212696, Aspira Pleural Drainage System
FDA 510(k), K212696, Aspira Pleural Drainage System
510(K) Number: K212696
Device Name: Aspira Pleural Drainage System
Manufacturer: Jennifer Webb
Device Classification Name: Apparatus, Suction, Patient Care
Regulation Number: DWM
Classification Product Code: KXA
Date Received: 08/25/2021
Decision Date: 03/03/2023
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Anesthesiology
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