Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K890514Substantially Equivalent

Pre-Moistened Cleansing Pad

Bausch & Lomb Incorporated, Rochester NY / Traditional, Substantially Equivalent

K890514 is the FDA 510(k) clearance record for PRE-MOISTENED CLEANSING PAD, cleared for Bausch & Lomb, Inc. on under FDA product code LKB (Pad, Alcohol, Device Disinfectant). FDA records list 131 510(k) clearances for Bausch & Lomb Incorporated, from to . As of , FDA records show no recalls naming K890514.

Clearance record

Decision date
Received
(68 days to decision)
Product code
LKB Pad, Alcohol, Device Disinfectant
Device class
Unclassified
Review panel
Unknown
Applicant
Bausch & Lomb, Inc. 1400 N. Goodman St., Rochester NY
Third party review
No

Clearances, product code LKB

Trailing 12 months

FDA records hold no clearances under product code LKB in the trailing twelve months.

FDA records show no clearances under product code LKB in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LKB, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260