NEOCOIL 3.0T 6-CHANNEL CAROTID ARRAY COIL— 510(k) K070778

Name: FDA 510(k) clearance K070778
Creator: U.S. Food and Drug Administration
Published: 2007-04-11

Substantially Equivalent

Neocoil

FDA 510(k) clearance K070778 for NEOCOIL 3.0T 6-CHANNEL CAROTID ARRAY COIL, Substantially Equivalent on 2007-04-11. Applicant: Neocoil. Device class: 2.

Clearance details

Applicant: Neocoil
Product code: Code MOS
Device class: Class 2
Regulation: 21 CFR 892.1000
Advisory panel: Radiology
Date received: 2007-03-21
Decision date: 2007-04-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pewaukee, WI, 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.