Product code LFJ— Gastroenterology, Urology

ADULT PERM-CATH 40CM.

Classification name
Catheter, Subclavian
Device class
Class 2
Regulation
21 CFR 876.5540
Advisory panel
Gastroenterology, Urology
Total cleared
65
First cleared
Most recent

Market context for product code LFJ

FDA has cleared 65 devices under product code LFJ between 1980 and 1994, filed by 22 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 LFJ

Recent clearances under product code LFJ

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