Interrad Medical, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K210629SecurAcathApril 12, 2021
K180994SecurAcath 10F, SecurAcath 12F, SecurAcath 5F, SecurAcath 5F, SecurAcath 6F, SecurAcath 7F/SecurAcatJuly 9, 2019
K180769SecurAcathJune 26, 2018
K120935SECURACATHApril 27, 2012
K092306SECURACATH UNIVERSALJuly 9, 2010
K083081MODIFICATION TO SECURACATH, MODEL: SPK01March 4, 2009
K082047SECURACATH CATHETER, MODEL SPK01September 30, 2008