FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇹 Italy

TEMPOROMANIBULAR COIL 15

K Number: K110373 · Decision Apr 6, 2011
Classifications
1
FEI Numbers
75
Registration Numbers
75
Same Product Code
487
Applicant Total
67
Review Days
57

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Basic Information

Device Name
TEMPOROMANIBULAR COIL 15
K Number
K110373
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1000
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Esaote, S.p.A.
Date Received
February 8, 2011
Decision Date
April 6, 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

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Other Clearances by Esaote, S.p.A.

K Number Device Name
K253288 6450 Ultrasound System (MyLabE80); 6450 Ultrasound System (MyLabE85)
K260746 S-scan Open (100001800)
K251901 Magnifico Open (100009900)
K253310 7600 Ultrasound System (MyLabC25); 7600 Ultrasound System (MyLabC30)
K243253 6600 Ultrasound System (MyLabA50); 6600 Ultrasound System (MyLabA70)
K241671 6450 Ultrasound System (MyLabE80); 6450 Ultrasound System (MyLabE85)
K241133 Magnifico Open (100009900); Magnifico MSK ( 100009910)
K230179 6440 MyLabX90
K212419 Magnifico Open, Magnifico MSK
K212021 6430 MyLabX75, 6430 MyLab XPro75
Search all 67 clearances from Esaote, S.p.A. →