FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇰 Denmark

TITAN

K Number: K103760 · Decision May 5, 2011
Classifications
1
FEI Numbers
57
Registration Numbers
57
Same Product Code
75
Applicant Total
17
Review Days
133

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Basic Information

Device Name
TITAN
K Number
K103760
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1900
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Interacoustics A/S
Date Received
December 23, 2010
Decision Date
May 5, 2011
Product Code
GWJ
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GWJ Stimulator, Auditory, Evoked Response

Similar 510(k) Clearances

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

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Other Clearances by Interacoustics A/S

K Number Device Name
K200534 VisualEyes
K200529 Orion
K192652 TRV
K191372 Lyra
K173567 Sera
K163149 VisualEyes
K162037 Eclipse with VEMP
K152112 VisualEyes
K151616 AT235
K131681 EYESEECAM VHIT
Search all 17 clearances from Interacoustics A/S →