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Overbed Table

Dynarex Corporation · Model 10450 · UDI-DI 00616784045016

INW
10
510(k) clearances
16
Adverse events (2 deaths)
1
Recalls
102
Facilities

Description

Overbed Table, H Base, Silver Vein, Walnut

Recalls

DateFirmReason
2003-05-30Chattanooga Corp.Product contains an improper bracket for the transducer.

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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.