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

Sirius MRI Marker NS

K Number: K171487 · Decision Aug 25, 2017
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
150
Applicant Total
4
Review Days
95

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Basic Information

Device Name
Sirius MRI Marker NS
K Number
K171487
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5730
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
C4 Imaging, LLC
Date Received
May 22, 2017
Decision Date
August 25, 2017
Product Code
KXK
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
KXK Source, Brachytherapy, Radionuclide

Similar 510(k) Clearances

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Other Clearances by C4 Imaging, LLC

K Number Device Name
K192771 C4 Fiducial Marker
K180069 HDR MRI Lumen Marker
K131689 MRI MARKER