Product code LJT— General Hospital

LOW PROFILE TITANIUM MODEL CATALOG #1003

Classification name
Port & Catheter, Implanted, Subcutaneous, Intravascular
Device class
Class 2
Regulation
21 CFR 880.5965
Advisory panel
General Hospital
Total cleared
288
First cleared
Most recent

Market context for product code LJT

FDA has cleared 288 devices under product code LJT between 1983 and 2026, filed by 80 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

Clearances per year

last 15 years

Top applicants under product code LJT

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, 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 →

Recent clearances under product code LJT

1–100 of 288

Data sourced from openFDA. This site is unofficial and independent of the FDA.