Upstream Peripheral Technologies, Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K211802GoBack Crossing CatheterMarch 1, 2022
K182937Upstream GoBack Crossing CatheterMay 23, 2019
K120964UPSTREAM GR CATHETERMay 25, 2012
K112887UPSTREAM NEEDLE HOLDER, UPSTREAM NEEDLE HOLDER WITH SHUT-OFF CONNECTORMarch 21, 2012
K112886UPSTREAM SUPPORT CATHETERFebruary 23, 2012