BARDEX ALL SILICONE PEDIATRIC CATHETER— 510(k) K821745
Substantially EquivalentC.R. Bard, Inc.
FDA 510(k) clearance K821745 for BARDEX ALL SILICONE PEDIATRIC CATHETER, Substantially Equivalent on 1982-06-24. Applicant: C.R. Bard, Inc.. Device class: 2.
Clearance details
- Applicant
- C.R. Bard, Inc.
- Product code
- Code KOD
- Device class
- Class 2
- Regulation
- 21 CFR 876.5130
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Warrendale, PA, US
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Adverse events under product code KOD
product code KOD- Death
- 5
- Injury
- 1,129
- Malfunction
- 7,019
- Total
- 8,153
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Recalls naming K821745
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K821745.
Data sourced from openFDA. This site is unofficial and independent of the FDA.