CATARACT LIQUEFRACTURE DEVICE— 510(k) K980292

Name: FDA 510(k) clearance K980292
Creator: U.S. Food and Drug Administration
Published: 1998-05-19

Substantially Equivalent

Alcon Laboratories

FDA 510(k) clearance K980292 for CATARACT LIQUEFRACTURE DEVICE, Substantially Equivalent on 1998-05-19. Applicant: Alcon Laboratories. Device class: 2.

Clearance details

Applicant: Alcon Laboratories
Product code: Code MUS
Device class: Class 2
Regulation: 21 CFR 886.4670
Advisory panel: Ophthalmic
Date received: 1998-01-26
Decision date: 1998-05-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fort Worth, TX, US

Download summary PDF View on FDA.gov ↗

More clearances from Alcon Laboratories

view all

K062624 — NEXT GENERATION LASER2007-11-05
K062865 — SMALL VOLUME SYRINGE2007-08-23
K000148 — RGP MULTI-PURPOSE SOLUTION ID 1001362000-04-11
K984573 — OPTI-FREE EXPRESS MULTI-ACTION CLEANING AND REWETTING DROP1999-09-16
K990480 — OPTI-FREE SUPRACLENS DAILY PROTEIN REMOVER1999-05-10

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