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

MULTIARRAY KIT

K Number: K121249 · Decision Jun 12, 2012
Classifications
1
FEI Numbers
75
Registration Numbers
75
Same Product Code
487
Applicant Total
8
Review Days
48

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Basic Information

Device Name
MULTIARRAY KIT
K Number
K121249
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.1000
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Paramed S.R.L.
Date Received
April 25, 2012
Decision Date
June 12, 2012
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 Paramed S.R.L.

K Number Device Name
K151466 MrOpen
K122034 MRJ 3300
K101295 MROPEN
K100164 MR INSPIRE WITH EXTENDED KIT
K073362 MROPEN
K080098 MRJ EXTENDED
K033507 MRJ