PowerGlide Pro Midline Catheter— 510(k) K153280

Substantially Equivalent

C.R. Bard, Inc.

FDA 510(k) clearance K153280 for PowerGlide Pro Midline Catheter, Substantially Equivalent on 2016-06-02. Applicant: C.R. Bard, Inc..

Clearance details

Applicant: C.R. Bard, Inc.
Product code: Code FOZ
Advisory panel: General Hospital
Date received: 2015-11-12
Decision date: 2016-06-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake Ciy,, UT, US

Download summary PDF View on FDA.gov ↗

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, 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.