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Wound Drain Catheter System

FDA product code OTK · Class 2 · General, Plastic Surgery

24

Registered devices

34

Adverse events

0

Recalls

7

510(k) clearances

Devices with this code

Pleuraflow® System with FlowGlide — Clearflow, Inc.Pleuraflow® System with FlowGlide — Clearflow, Inc.PleuraFlow® System — Clearflow, Inc.PleuraFlow® System with FlowGlide — Clearflow, Inc.PleuraFlow® System — Clearflow, Inc.PleuraFlow® ZIP — Clearflow, Inc.Pleuraflow® System with FlowGlide — Clearflow, Inc.Pleuraflow® System with FlowGlide — Clearflow, Inc.PleuraFlow® System with FlowGlide — Clearflow, Inc.Pleuraflow® System with FlowGlide — Clearflow, Inc.PleuraFlow® System with FlowGlide — Clearflow, Inc.PleuraFlow® System with FlowGlide — Clearflow, Inc.PleuraFlow® System with FlowGlide — Clearflow, Inc.PleuraFlow® System — Clearflow, Inc.PleuraFlow® System — Clearflow, Inc.Pleuraflow® System with FlowGlide — Clearflow, Inc.PleuraFlow® System with FlowGlide — Clearflow, Inc.PleuraFlow® System with FlowGlide — Clearflow, Inc.PleuraFlow® System with FlowGlide — Clearflow, Inc.PleuraFlow® System with FlowGlide — Clearflow, Inc.Pleuraflow® System with FlowGlide — Clearflow, Inc.Pleuraflow® System with FlowGlide — Clearflow, Inc.PleuraFlow® System with FlowGlide — Clearflow, Inc.Pleuraflow® System with FlowGlide — Clearflow, Inc.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.