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FDA 510(k) Applications Submitted by Alexandra Hyde
FDA 510(k) Number
Submission Date
Device Name
Applicant
K250891
03/25/2025
Cure Catheter Insertion Kit (K1); Cure Catheter Insertion Kit (K2); Cure Catheter Insertion Kit (K2-90); Cure Catheter Insertion Kit (K3); Cure Hydrophilic Catheter Kit (HM12UK); Cure Hydrophilic Catheter Kit (HM14UK); Cure Hydrophilic Catheter Kit (HM16U
ConvaTec Limited
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