POWERPORT IMPLANTABLE PORT— 510(k) K133335

Substantially Equivalent

C.R. Bard, Inc.

FDA 510(k) clearance K133335 for POWERPORT IMPLANTABLE PORT, Substantially Equivalent on 2014-02-14. Applicant: C.R. Bard, Inc..

Clearance details

Applicant: C.R. Bard, Inc.
Product code: Code LJT
Advisory panel: General Hospital
Date received: 2013-10-29
Decision date: 2014-02-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake Ciy,, UT, US

Download summary PDF View on FDA.gov ↗

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, 2020-01-01 through 2026-04-23. 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.