PATHFINDER— 510(k) K910601

Substantially Equivalent

Nurion Industries

FDA 510(k) clearance K910601 for PATHFINDER, Substantially Equivalent on 1991-05-14. Applicant: Nurion Industries. Device class: 1.

Clearance details

Applicant: Nurion Industries
Product code: Code HPG
Device class: Class 1
Regulation: 21 CFR 886.5900
Advisory panel: Ophthalmic
Date received: 1991-02-13
Decision date: 1991-05-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Paoli, PA, 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.