CORRIDOR4DM— 510(k) K080575

Substantially Equivalent

Invia

FDA 510(k) clearance K080575 for CORRIDOR4DM, Substantially Equivalent on 2008-05-13. Applicant: Invia. Device class: 2.

Clearance details

Applicant: Invia
Product code: Code KPS
Device class: Class 2
Regulation: 21 CFR 892.1200
Advisory panel: Radiology
Date received: 2008-02-29
Decision date: 2008-05-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ashland, MA, 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.