BD L-CATH SINGLE AND DUAL LUMENT CATHETERS, MIDLINE CATHETER— 510(k) K091670
Substantially EquivalentBecton, Dickinson & CO
FDA 510(k) clearance K091670 for BD L-CATH SINGLE AND DUAL LUMENT CATHETERS, MIDLINE CATHETER, Substantially Equivalent on 2009-07-01. Applicant: Becton, Dickinson & CO.
Clearance details
- Applicant
- Becton, Dickinson & CO
- Product code
- Code LJS
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Sandy, UT, US
Adverse events under product code LJS
product code LJS- Death
- 31
- Injury
- 2,791
- Malfunction
- 18,374
- Other
- 5
- Total
- 21,201
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 →
Data sourced from openFDA. This site is unofficial and independent of the FDA.