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NIHON KOHDEN AMERICA, INC. · Model JE-227AK · UDI-DI 00841983102479

OLTGWQGYC Prescription
10
510(k) clearances
35
Adverse events (2 deaths)
0
Recalls
67
Facilities

Description

Flat Pack Mini Expansion, Channel 129-192

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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.