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PleuraFlow® System

Clearflow, Inc. · Model PF-32 · UDI-DI 00856449006031

OTK Prescription
7
510(k) clearances
34
Adverse events (1 deaths)
0
Recalls
2
Facilities

Description

PF-32 PleuraFlow® System

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.