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FDA PRODUCT CODE · CLASS III

QZV — Pediatric Extracorporeal Synthetic Semipermeable Membrane Cartridge For Acute Kidney Injury

For the treatment of acute kidney injury in pediatric patients, in conjunction with continuous kidney replacement treatment (CKRT).

DEVICE CLASS
Class III
MEDICAL SPECIALTY
Unknown
REVIEW PANEL
HE
— Implant✓ Life-sustaining— GMP-exempt— Third-party review eligible
0
510(K)/PMA CLEARANCES
0
RECALL ENTRIES

Related on SPEQ

Medical devices industry →Medical device quality (ISO 13485) →FDA device clearances →FDA enforcement & recalls →

Source: FDA device classification, 510(k)/PMA, and recall datasets (openFDA). Recall entries count distinct FDA recall numbers, so one recall event affecting several products appears as several entries. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data.

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