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

MRT-50A MOBILE

K Number: K893750 · Decision Aug 9, 1989
Classifications
1
FEI Numbers
146
Registration Numbers
146
Same Product Code
1098
Applicant Total
54
Review Days
83

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Basic Information

Device Name
MRT-50A MOBILE
K Number
K893750
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1000
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Toshiba Medical Systems
Date Received
May 18, 1989
Decision Date
August 9, 1989
Product Code
LNH
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
LNH System, Nuclear Magnetic Resonance Imaging

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K891453 DIAGNOSTIC ULTRASOUND TRANSDUCER: PVE-582V
K890969 TRANSESOPHAGEAL TRANSDUCER PEF-511SA
K884555 TCT-600HQ COMPU TOMO(CT)XRAY/HEAD/WHOLE BODY EXAM
K884788 TOSHIBA TCT-600XT COMPUTED TOMOGRAPHY X-RAY SYSTEM
K883359 DIAGNOSTIC ULTRASOUND SYSTEM SSA-270A
K883756 TOSHIBA MRT-50A MAGNETIC RESONANCE SYSTEM
K881305 TCT-300S COMPUTED TOMO. (CT) X-RAY SYSTEM FOR EXAM
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