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

ATAMA SYSTEM

K Number: K132444 · Decision Jan 27, 2014
Classifications
1
FEI Numbers
75
Registration Numbers
75
Same Product Code
487
Applicant Total
11
Review Days
174

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Basic Information

Device Name
ATAMA SYSTEM
K Number
K132444
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1000
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Monteris Medical,
Date Received
August 6, 2013
Decision Date
January 27, 2014
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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