OP-2 (LOTIFOCON B) & OP-6 (LOTIFOCON C)— 510(k) K952260

Name: FDA 510(k) clearance K952260
Creator: U.S. Food and Drug Administration
Published: 1996-01-03

Substantially Equivalent

Stellar Contact Lens, Inc.

FDA 510(k) clearance K952260 for OP-2 (LOTIFOCON B) & OP-6 (LOTIFOCON C), Substantially Equivalent on 1996-01-03. Applicant: Stellar Contact Lens, Inc.. Device class: 2.

Clearance details

Applicant: Stellar Contact Lens, Inc.
Product code: Code HQD
Device class: Class 2
Regulation: 21 CFR 886.5916
Advisory panel: Ophthalmic
Date received: 1995-05-15
Decision date: 1996-01-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chicago, IL, 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.