ALCON SITE(R)-COMPATIBLE CASSETTE— 510(k) K881682

Name: FDA 510(k) clearance K881682
Creator: U.S. Food and Drug Administration
Published: 1988-07-01

Substantially Equivalent

Alcon Laboratories

FDA 510(k) clearance K881682 for ALCON SITE(R)-COMPATIBLE CASSETTE, Substantially Equivalent on 1988-07-01. Applicant: Alcon Laboratories. Device class: 1.

Clearance details

Applicant: Alcon Laboratories
Product code: Code KYG
Device class: Class 1
Regulation: 21 CFR 886.4360
Advisory panel: Ophthalmic
Date received: 1988-04-19
Decision date: 1988-07-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fort Worth, TX, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KYG

view all

K010353 — MED-LOGICS DISPOSABLE ALK TUBING2001-04-27
K003036 — TURBO-FLOW INFUSION CANNULA 19 GAGE,20 GAGE,23 GAGE, 25 GAGE, MODEL 101019,101020,101023,1010252000-12-22
K993591 — BLADEWORKS DISPOSABLE ALK TUBING1999-12-28
K981116 — SOVEREIGN CATARACT EXTRACTION SYSTEM1998-05-19
K980647 — EYE IRRIGATOR MODEL #20201998-05-15

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.