IKOENGELO— 510(k) K061006

Substantially Equivalent

Ikoetech, LLC

FDA 510(k) clearance K061006 for IKOENGELO, Substantially Equivalent on 2006-06-05. Applicant: Ikoetech, LLC.

Clearance details

Applicant: Ikoetech, LLC
Product code: Code KPQ
Advisory panel: Radiology
Date received: 2006-04-11
Decision date: 2006-06-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Houston, TX, US

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