CATHTONG™ II PICC Catheter— 510(k) K232571

Substantially Equivalent

L&Z Us, Inc.

FDA 510(k) clearance K232571 for CATHTONG™ II PICC Catheter, Substantially Equivalent on 2023-09-22. Applicant: L&Z Us, Inc..

Clearance details

Applicant
L&Z Us, Inc.
Product code
Code LJS
Advisory panel
General Hospital
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Special
Location
Norwood, NJ, US
Download summary PDFView 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, 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.