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GE Healthcare Finland Oy · Model Pedi-lite Spirometry Kit 2m, 8002718 · UDI-DI 00840682102865

CAP CBS BZL NHP CBQ CBR BZK NHO CCL NHQ CCK Prescription

510(k) clearances

Adverse events (10 deaths)

Recalls

Facilities

Description

PEDI-LITE+ SPIROMETRY KIT 2M/7FT, 8002718

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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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.