Pathway, LLC
FDA Regulatory Profile
Pathway, LLC appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on April 21, 2020.
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 |