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CHATTANOOGA

DJO, LLC · Model 15-0160 · UDI-DI 00190446780304

IMG Prescription
10
510(k) clearances
235
Adverse events (2 deaths)
2
Recalls
23
Facilities

Description

G16 ULTRASOUND APPLICATOR 1 CM2 USA

Recalls

DateFirmReason
2008-02-28Chattanooga Corp IncDevice may fail to administer therapy during use.
2008-02-28Chattanooga Corp IncDevice may fail to administer therapy during use.

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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.