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

INTERA-SENSATION FAMILY

K Number: K031815 · Decision Sep 10, 2003
Classifications
1
FEI Numbers
146
Registration Numbers
146
Same Product Code
1098
Applicant Total
107
Review Days
90

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Basic Information

Device Name
INTERA-SENSATION FAMILY
K Number
K031815
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1000
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Philips Medical Systems
Date Received
June 12, 2003
Decision Date
September 10, 2003
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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