TBD KERATOSCOPE— 510(k) K912130

Substantially Equivalent

Alcon Laboratories

FDA 510(k) clearance K912130 for TBD KERATOSCOPE, Substantially Equivalent on 1991-08-09. Applicant: Alcon Laboratories. Device class: 1.

Clearance details

Applicant: Alcon Laboratories
Product code: Code HLQ
Device class: Class 1
Regulation: 21 CFR 886.1350
Advisory panel: Ophthalmic
Date received: 1991-05-14
Decision date: 1991-08-09
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.