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Variants of OPTIBOND by Kerr Corporation (Danbury)
2 variants
Key
Device
Device · Manufacturer · Authorizations
Verified
Verified
Status
Status
Regime
Regime
Registry
Registry
Class
Class
Optibond
Kerr Corporation (Danbury)
·
,
United States
(FDA applicant)
FDA 510(k)
K940513
Active
Cleared 15 Apr 1994
Active
Regimes:
510(k)
Registry:
510(k)
Class
Class:
II
Optibond
Kerr Corporation (Danbury)
·
,
United States
(FDA applicant)
FDA 510(k)
K923546
Active
Cleared 29 Sep 1992
Active
Regimes:
510(k)
Registry:
510(k)
Class
Class:
II
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