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Coloplast Manufacturing Us, LLC

FDA 510(k) & PMA Approved Devices — 4 products

Total Devices4
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K100878 SELF CATH CATHETEREZD2010-05-26 View
510(k) K093112 DIGITEX SUTURE DELIVERY SYSTEM, MODEL 52025, DIGITEX SUTURE CARTRIDGE (SIZE O), MODEL 52026, DIGITEX SUTURE CARTRIDGEGAW2010-02-01 View
510(k) K082640 VIRTUE VENTRAL URETHRAL ELEVATION SLING SYSTEMOTM2008-10-17 View
510(k) K070939 SELF-CATH CS CLOSED URINARY CATHETERIZATION SYSTEMFCM2007-06-01 View
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