KERATRON CORNEAL TOPOGRAPHER— 510(k) K944616

Name: FDA 510(k) clearance K944616
Creator: U.S. Food and Drug Administration
Published: 1994-11-22

Substantially Equivalent

Alliance Medical Marketinig

FDA 510(k) clearance K944616 for KERATRON CORNEAL TOPOGRAPHER, Substantially Equivalent on 1994-11-22. Applicant: Alliance Medical Marketinig. Device class: 1.

Clearance details

Applicant: Alliance Medical Marketinig
Product code: Code HLQ
Device class: Class 1
Regulation: 21 CFR 886.1350
Advisory panel: Ophthalmic
Date received: 1994-09-20
Decision date: 1994-11-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jacksonville Beach, FL, US

Download summary PDF View on FDA.gov ↗

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K944207 — TOPOGRAPHIC MODELING SYSTEM 2 TMS-21994-12-07

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