CAREVENT— 510(k) K062240

Substantially Equivalent

Chief Medical, LLC

FDA 510(k) clearance K062240 for CAREVENT, Substantially Equivalent on 2006-10-16. Applicant: Chief Medical, LLC. Device class: 2.

Clearance details

Applicant: Chief Medical, LLC
Product code: Code KNY
Device class: Class 2
Regulation: 21 CFR 876.5130
Advisory panel: Gastroenterology, Urology
Date received: 2006-08-02
Decision date: 2006-10-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Teton Village, WY, 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.