OPTI-FREE SUPRACLENS DAILY POTEIN REMOVER / RGP MULTI-PURPOSE DISINFECTING SOLUTION ID 100136— 510(k) K001235

Name: FDA 510(k) clearance K001235
Creator: U.S. Food and Drug Administration
Published: 2000-07-03

Substantially Equivalent

Alcon Universal, Ltd.

FDA 510(k) clearance K001235 for OPTI-FREE SUPRACLENS DAILY POTEIN REMOVER / RGP MULTI-PURPOSE DISINFECTING SOLUTION ID 100136, Substantially Equivalent on 2000-07-03. Applicant: Alcon Universal, Ltd.. Device class: 2.

Clearance details

Applicant: Alcon Universal, Ltd.
Product code: Code MRC
Device class: Class 2
Regulation: 21 CFR 886.5918
Advisory panel: Ophthalmic
Date received: 2000-04-17
Decision date: 2000-07-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fort Worth, TX, US

Download summary PDF View on FDA.gov ↗

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