PORT-A-CATH DUAL LUMEN IMPLANTABLE VENOUS ACCESS— 510(k) K932841
Substantially EquivalentPharmacia Deltec, Inc.
FDA 510(k) clearance K932841 for PORT-A-CATH DUAL LUMEN IMPLANTABLE VENOUS ACCESS, Substantially Equivalent on 1994-01-05. Applicant: Pharmacia Deltec, Inc..
Clearance details
- Applicant
- Pharmacia Deltec, Inc.
- Product code
- Code LJT
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- St. Paul, MN, US
Adverse events under product code LJT
product code LJT- Death
- 234
- Injury
- 6,468
- Malfunction
- 5,326
- Other
- 2
- Total
- 12,030
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.