DeviceClearance

Product code JOW— Cardiovascular

REPROCESSED COMPRESSION SLEEVES

Classification name
Sleeve, Limb, Compressible
Device class
Class 2
Regulation
21 CFR 870.5800
Advisory panel
Cardiovascular
Total cleared
354
First cleared
Most recent

Market context for product code JOW

FDA has cleared 354 devices under product code JOW between 1977 and 2026, filed by 169 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 JOW

Recent clearances under product code JOW

1–100 of 354

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