MEDTRONIC SOLAN FIBEROPTIC CORNEAL LIGHT PROBE— 510(k) K000728

Name: FDA 510(k) clearance K000728
Creator: U.S. Food and Drug Administration
Published: 2000-03-21

Substantially Equivalent

Medtronic Xomed

FDA 510(k) clearance K000728 for MEDTRONIC SOLAN FIBEROPTIC CORNEAL LIGHT PROBE, Substantially Equivalent on 2000-03-21. Applicant: Medtronic Xomed. Device class: 2.

Clearance details

Applicant: Medtronic Xomed
Product code: Code FST
Device class: Class 2
Regulation: 21 CFR 878.4580
Advisory panel: General, Plastic Surgery
Date received: 2000-03-06
Decision date: 2000-03-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jacksonville, FL, 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.