FDA 510(k) FDA unclassified Substantially Equivalent 🇩🇰 Denmark

TRV

K Number: K192652 · Decision May 27, 2020
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
21
Applicant Total
17
Review Days
246

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
TRV
K Number
K192652
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Interacoustics A/S
Date Received
September 24, 2019
Decision Date
May 27, 2020
Product Code
LXV
Advisory Committee
Unknown
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
LXV Apparatus, Vestibular Analysis

Similar 510(k) Clearances

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

View all

Other Clearances by Interacoustics A/S

K Number Device Name
K200534 VisualEyes
K200529 Orion
K191372 Lyra
K173567 Sera
K163149 VisualEyes
K162037 Eclipse with VEMP
K152112 VisualEyes
K151616 AT235
K131681 EYESEECAM VHIT
K130795 TITAN
Search all 17 clearances from Interacoustics A/S →