Skip to content
devi
CERTS
Devices
Categories
Manufacturers
Importers
Certifiers
Authorities
Reps.
Representatives
Results for “audifon vico M TRT”
Name, manufacturer or identifier
Search
Manufacturer
(optional)
Filters
Filters
Registry
EUDAMED
FDA 510(k) incl. De Novo
1
FDA PMA
GUDID
4
Country / market
United States
5
Risk class
Class I
Class IIa
Class IIb
Class III
Class II (US)
5
More classes (11)
Class A
Class B
Class C
Class D
IVD General
IVD Annex II List A
IVD Annex II List B
IVD for self-testing
Active implantable (AIMDD)
Unclassified (FDA)
Not classified (FDA)
Verified
Verified only
Category (EMDN)
Browse by category
Apply filters
5 devices found
·
sorted by relevance
Key
Clear all
Device
Device · Manufacturer · Authorizations
Verified
Verified
Status
Status
Regime
Regime
Registry
Registry
Class
Class
audifon vico M TRT
audifon GmbH & Co. KG
·
,
FDA registration: United States
Group of variants
GUDID
not on market
Withdrawn
Registry:
GUDID
Class
Class:
II
Audifon Arriva Cic, Is, Is+, M, S, S+, X Trt, Audifon Vico, Audifon Prado, Audifon Elia, Cic, Is, Is+, M, S Trt
Audifon-USA, Inc.
·
,
United States
(FDA applicant)
FDA 510(k)
K130514
Active
Cleared 21 Nov 2013
Active
Regimes:
510(k)
Registry:
510(k)
Class
Class:
II
Previous
Next
Showing 1-5 of 5