Biowy PlCC Catheter— 510(k) K173956

Substantially Equivalent

Biowy Corporation

FDA 510(k) clearance K173956 for Biowy PlCC Catheter, Substantially Equivalent on 2018-05-21. Applicant: Biowy Corporation.

Clearance details

Applicant: Biowy Corporation
Product code: Code LJS
Advisory panel: General Hospital
Date received: 2017-12-28
Decision date: 2018-05-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lake Forest, CA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code LJS

product code LJS

Death: 31
Injury: 2,791
Malfunction: 18,374
Other: 5
Total: 21,201

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.