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Medron, LLC

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
5
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K192283MEDRON Vessel Dilator - 6F x 22cm HDPE Dilator, MEDRON Vessel Dilator - 15.5F - 17.5F HDPE DilatorMay 6, 2020
K971897CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATHETER 10 FR (CAVH)October 21, 1997
K940775INJECTION CAPJune 15, 1994