510(k) K172289
K172289 is an FDA 510(k) premarket notification submitted by Q Urological Corporation for the device "pAguaMedicina PERSISTENT Structural Hydrogel Ureteral Stent". The FDA issued a decision of Substantially Equivalent on Oct 4, 2017. The device falls under product code FAD (Stent, Ureteral), a Class II device regulated under 21 CFR 876.4620. Q Urological Corporation has 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Oct 4, 2017
- Date Received
- Jul 31, 2017
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Stent, Ureteral
- Device Class
- Class II
- Regulation Number
- 876.4620
- Review Panel
- GU
- Submission Type
- 510(k)