DeviceClearance

Product code LCC— Ophthalmic

WEE BAG O'MERCURY

Classification name
Applicator, Ocular Pressure
Device class
Class 2
Regulation
21 CFR 886.4610
Advisory panel
Ophthalmic
Total cleared
6
First cleared
Most recent

Market context for product code LCC

FDA has cleared 6 devices under product code LCC between 1979 and 2012, filed by 6 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

Top applicants under product code LCC

Recent clearances under product code LCC

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