510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K980292Substantially Equivalent

Cataract Liquefracture Device

Alcon Laboratories, Fort Worth TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K980292 is the FDA 510(k) clearance record for CATARACT LIQUEFRACTURE DEVICE, a class II device, cleared for Alcon Laboratories on under FDA product code MUS (Fluidic, Phacoemulsification/Phacofragmentation). FDA records list 152 510(k) clearances for Alcon Laboratories, from to . As of , FDA records show no recalls naming K980292.

Clearance record

Decision date
Received
(113 days to decision)
Product code
MUS Fluidic, Phacoemulsification/Phacofragmentation
Regulation
21 CFR 886.4670
Device class
Class II
Review panel
Ophthalmic
Applicant
Alcon Laboratories 6201 S. Fwy. R7-14, Fort Worth TX
510(k) summary
Summary
Third party review
No

Clearances, product code MUS

Trailing 12 months

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

FDA records show no clearances under product code MUS in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code MUS, 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