PANAG— 510(k) K011891

Substantially Equivalent

Panag International

FDA 510(k) clearance K011891 for PANAG, Substantially Equivalent on 2002-07-30. Applicant: Panag International. Device class: 2.

Clearance details

Applicant: Panag International
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2001-06-18
Decision date: 2002-07-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Johannesburg, ZA

Download summary PDF View on FDA.gov ↗

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