NEOCOIL 1.5T 16 CHANNEL CARDIAC-ABDOMINAL-PELVIC ARRAY COIL— 510(k) K073181

Name: FDA 510(k) clearance K073181
Creator: U.S. Food and Drug Administration
Published: 2007-11-21

Substantially Equivalent

Neocoil, LLC

FDA 510(k) clearance K073181 for NEOCOIL 1.5T 16 CHANNEL CARDIAC-ABDOMINAL-PELVIC ARRAY COIL, Substantially Equivalent on 2007-11-21. Applicant: Neocoil, LLC. Device class: 2.

Clearance details

Applicant: Neocoil, LLC
Product code: Code MOS
Device class: Class 2
Regulation: 21 CFR 892.1000
Advisory panel: Radiology
Date received: 2007-11-13
Decision date: 2007-11-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pewaukee, WI, US

Download summary PDF View on FDA.gov ↗

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