FOOTPRINT MEDICAL PERIPHERALLY INSERTED CENTRAL CATHETER, MODEL S1PIC1.9-C— 510(k) K091488

Substantially Equivalent

Footprint Medical

FDA 510(k) clearance K091488 for FOOTPRINT MEDICAL PERIPHERALLY INSERTED CENTRAL CATHETER, MODEL S1PIC1.9-C, Substantially Equivalent on 2009-09-14. Applicant: Footprint Medical.

Clearance details

Applicant: Footprint Medical
Product code: Code LJS
Advisory panel: General Hospital
Date received: 2009-05-19
Decision date: 2009-09-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Antonio, TX, 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.