FDA 510(k) Applications for Medical Device Product Code "KMK"
(Device, Intravascular Catheter Securement)

FDA 510(k) Number Applicant Device Name Decision Date
K963365 BYRD MEDICAL DEVICES, INC. MULTI-PURPOSE MEDICAL TUBE HOLDER 10/11/1996
K180994 Interrad Medical Inc SecurAcath 10F, SecurAcath 12F, SecurAcath 5F, SecurAcath 5F, SecurAcath 6F, SecurAcath 7F/SecurAcath 8F 07/09/2019
K981860 PARAWORKS ENTERPRISE, LTD. A P HARNESS 06/03/1999


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