FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

SV BRAIN ARRAY, SIEMENS 3T

K Number: K111802 · Decision Sep 8, 2011
Classifications
1
FEI Numbers
75
Registration Numbers
75
Same Product Code
487
Applicant Total
14
Review Days
73

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
SV BRAIN ARRAY, SIEMENS 3T
K Number
K111802
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1000
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Mri Interventions, Inc.
Date Received
June 27, 2011
Decision Date
September 8, 2011
Product Code
MOS
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MOS Coil, Magnetic Resonance, Specialty

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MOS), ordered by most recent decision date.

View all

Other Clearances by Mri Interventions, Inc.

K Number Device Name
K200079 ClearPoint System and Accessories
K191701 Arcus Head Fixation Frame
K191400 Voyager Trajectory Array Guide (V-TAG)
K181731 MR Compatible Aspiration Kit
K181195 ClearPoint System
K171257 ClearPoint System
K160129 MRII Cranial Drill and Accessories
K160434 ClearPoint System
K142505 ClearPoint System
K151536 SmartTwist MRII Hand Drill, SmartTip MRII Drill bit Kit, 4.5mm, 6.0mm
Search all 14 clearances from Mri Interventions, Inc. →