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DOPPLEX

HUNTLEIGH HEALTHCARE LIMITED · Model DFK2-USA-D900-P · UDI-DI 05051968017666

KNG Prescription
1
510(k) clearances
32
Adverse events (2 deaths)
1
Recalls
31
Facilities

Description

DIABETIC FOOT KIT-USA MINI DOPPLX

Recalls

DateFirmReason
2017-10-06CooperSurgical, Inc.The 2MHZ prove was incorrectlhttp://cts.fda.gov/division-tracking/images/trash.pngy labeled as a 3MHZ probe

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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.