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

TITAN

K Number: K121847 · Decision Nov 29, 2012
Classifications
1
FEI Numbers
13
Registration Numbers
13
Same Product Code
69
Applicant Total
17
Review Days
157

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Basic Information

Device Name
TITAN
K Number
K121847
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.1090
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Interacoustics A/S
Date Received
June 25, 2012
Decision Date
November 29, 2012
Product Code
ETY
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

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

Product Code Device Name
ETY Tester, Auditory Impedance

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (ETY), 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 →