FDA 510(k) FDA class 2 Substantially Equivalent 🇳🇴 Norway

fMRI Hardware System

K Number: K232680 · Decision Dec 13, 2023
Classifications
1
FEI Numbers
146
Registration Numbers
146
Same Product Code
1098
Applicant Total
7
Review Days
103

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Basic Information

Device Name
fMRI Hardware System
K Number
K232680
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1000
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nordicneurolab AS
Date Received
September 1, 2023
Decision Date
December 13, 2023
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LNH), ordered by most recent decision date.

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Other Clearances by Nordicneurolab AS

K Number Device Name
K251937 nordicAudio (1.0)
K243209 nordicMEDiVA
K241608 nordicMEDiVA
K212720 nordicDSC
K191032 fMRI Hardware System
K163324 nordicBrainEx