THE PATHFINDER SYSTEM— 510(k) K890483

Substantially Equivalent

Denmark Assoc.

FDA 510(k) clearance K890483 for THE PATHFINDER SYSTEM, Substantially Equivalent on 1989-03-14. Applicant: Denmark Assoc.. Device class: 2.

Clearance details

Applicant: Denmark Assoc.
Product code: Code IZH
Device class: Class 2
Regulation: 21 CFR 892.1710
Advisory panel: Radiology
Date received: 1989-01-31
Decision date: 1989-03-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bowling Green, KY, 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.