FDA 510(k) K221365, LapBox Tissue Containment Removal System, ProMedoss, Inc.

FDA 510(k) K221365, LapBox Tissue Containment Removal System, ProMedoss, Inc.

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510(K) Number: K221365
Device Name: LapBox Tissue Containment Removal System
Manufacturer: ProMedoss, Inc.
Device Classification Name: Laparoscope, General & Plastic Surgery
Regulation Number: 876.1500
Classification Product Code: GCJ
Date Received: 05/12/2022
Decision Date: 08/25/2022
Regulation Medical Specialty: General & Plastic Surgery
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