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

MRI PATIENT POSITIONING DEVICES

K Number: K093738 · Decision May 14, 2010
Classifications
1
FEI Numbers
146
Registration Numbers
146
Same Product Code
1098
Applicant Total
41
Review Days
161

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Basic Information

Device Name
MRI PATIENT POSITIONING DEVICES
K Number
K093738
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1000
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medtec, Inc.
Date Received
December 4, 2009
Decision Date
May 14, 2010
Product Code
LNH
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
Y

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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