PowerGlide Pro Midline Catheter— 510(k) K240359
Substantially EquivalentBecton, Dickinson and Company (Bard Access Systems, Inc.)
FDA 510(k) clearance K240359 for PowerGlide Pro Midline Catheter, Substantially Equivalent on 2024-07-29. Applicant: Becton, Dickinson and Company (Bard Access Systems, Inc.).
Clearance details
- Applicant
- Becton, Dickinson and Company (Bard Access Systems, Inc.)
- Product code
- Code FOZ
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Salt Lake City, UT, US
Adverse events under product code FOZ
product code FOZ- Death
- 38
- Injury
- 2,290
- Malfunction
- 25,858
- Other
- 11
- Total
- 28,197
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.