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Variants of URETERAL DILATOR by American Edwards Laboratories
2 variants
Key
Device · Manufacturer · Authorizations
Verified
Status
Regime
Registry
Class
Ureteral Dilator
American Edwards Laboratories
·
,
FDA registration: United States
Class II
FDA 510(k)
K852324
Active
Cleared 21 Aug 1985
Active
510(k)
510(k)
II
Ureteral Dilator
American Edwards Laboratories
·
,
FDA registration: United States
Class II
FDA 510(k)
K840746
Active
Cleared 13 Apr 1984
Active
510(k)
510(k)
II
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