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Variants of SECULOK™ ACP System by U&I Corporation
2 variants
Key
Device · Manufacturer · Authorizations
Verified
Status
Regime
Registry
Class
SECULOK™ ACP System
U&I Corporation
·
,
FDA registration: United States
Class II
FDA 510(k)
K182055
Active
Cleared 10 Sep 2018
Active
510(k)
510(k)
II
SECULOK™ ACP System
U&I Corporation
·
,
FDA registration: United States
Class II
FDA 510(k)
K190053
Active
Cleared 1 Feb 2019
Active
510(k)
510(k)
II
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