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Variants of OTICON by Oticon, Inc.
2 variants
Key
Device
Device · Manufacturer · Authorizations
Verified
Verified
Status
Status
Regime
Regime
Registry
Registry
Class
Class
Oticon
Oticon, Inc.
·
,
FDA registration: United States
FDA 510(k)
K954794
Active
Cleared 13 Nov 1995
Active
Regimes:
510(k)
Registry:
510(k)
Class
Class:
I
Oticon
Oticon, Inc.
·
,
FDA registration: United States
FDA 510(k)
K946045
Active
Cleared 30 Jan 1995
Active
Regimes:
510(k)
Registry:
510(k)
Class
Class:
I
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