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PTA Scoring Balloon Dilatation Catheter

DK Medical Technology Co., Ltd. · Model DKT35-5040B · UDI-DI 06972253606213

PNO
1
510(k) clearances
2,118
Adverse events (2 deaths)
3
Recalls
34
Facilities

Recalls

DateFirmReason
2019-05-24Cook Inc.Multiple complaints were received for balloons bursting below the rated burst pressure. Potential adverse events that may occur if an affected product is used include a delay in t
2019-05-24Cook Inc.Multiple complaints were received for balloons bursting below the rated burst pressure. Potential adverse events that may occur if an affected product is used include a delay in t
2019-05-24Cook Inc.Multiple complaints were received for balloons bursting below the rated burst pressure. Potential adverse events that may occur if an affected product is used include a delay in t

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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.