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Variants of AURORA by Aurora Imaging Technology, Inc.
2 variants
Key
Device
Device · Manufacturer · Authorizations
Verified
Verified
Status
Status
Regime
Regime
Registry
Registry
Class
Class
Aurora
Aurora Imaging Technology, Inc.
·
,
United States
(FDA applicant)
FDA 510(k)
K003651
Active
Cleared 21 Feb 2001
Active
Regimes:
510(k)
Registry:
510(k)
Class
Class:
II
Aurora
Aurora Imaging Technology, Inc.
·
,
United States
(FDA applicant)
FDA 510(k)
K032082
Active
Cleared 30 Jul 2003
Active
Regimes:
510(k)
Registry:
510(k)
Class
Class:
II
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