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Pathway, LLC
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K192034
HDX 100% Silicone 2-way Foley Catheter, 14Fr/10cc, HDX 100% Silicone 2-way Foley Catheter, 16Fr/5cc,
April 21, 2020
K181616
PSM 3-Way Silicone Foley Catheter
September 21, 2018
K162233
Kurin Blood Culture Collection Set
December 23, 2016