ANGIOCATH(R) NONVALON(R) AND ANGIO-SET(R) IV CATHETERS— 510(k) K950301
Substantially EquivalentBecton Dickinson Vascular Access, Inc.
FDA 510(k) clearance K950301 for ANGIOCATH(R) NONVALON(R) AND ANGIO-SET(R) IV CATHETERS, Substantially Equivalent on 1995-04-18. Applicant: Becton Dickinson Vascular Access, Inc..
Clearance details
- Applicant
- Becton Dickinson Vascular Access, Inc.
- Product code
- Code FOZ
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Sandy, 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.