510(k) K071311

NEOCOIL 1.5T 8-CHANNEL SHOULDER ARRAY COIL by Neocoil — Product Code MOS

K071311 is an FDA 510(k) premarket notification submitted by Neocoil for the device "NEOCOIL 1.5T 8-CHANNEL SHOULDER ARRAY COIL". The FDA issued a decision of Substantially Equivalent on May 22, 2007. The device falls under product code MOS (Coil, Magnetic Resonance, Specialty), a Class II device regulated under 21 CFR 892.1000. Neocoil has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 22, 2007
Date Received
May 9, 2007
Clearance Type
Traditional
Expedited Review
No
Third Party Review
Yes

Device Classification

Device Name
Coil, Magnetic Resonance, Specialty
Device Class
Class II
Regulation Number
892.1000
Review Panel
RA
Submission Type