TEARTEC RAPID LACRIMAL ASSESMENT SYSTEM— 510(k) K911734

Name: FDA 510(k) clearance K911734
Creator: U.S. Food and Drug Administration
Published: 1991-11-07

Substantially Equivalent

Northland Cataract & Eye Care Clinic

FDA 510(k) clearance K911734 for TEARTEC RAPID LACRIMAL ASSESMENT SYSTEM, Substantially Equivalent on 1991-11-07. Applicant: Northland Cataract & Eye Care Clinic. Device class: 1.

Clearance details

Applicant: Northland Cataract & Eye Care Clinic
Product code: Code KYD
Device class: Class 1
Regulation: 21 CFR 886.1800
Advisory panel: Ophthalmic
Date received: 1991-04-17
Decision date: 1991-11-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kansas City, MO, US

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