Dislodger, Stone, Flexible, Ureteral, Reprocessed
NQT is the FDA product code for Dislodger, Stone, Flexible, Ureteral, Reprocessed, a class II device type, regulated under 21 CFR 876.4680. FDA's definition for this code reads: "A ureteral stone dislodger is a device that consists of a bougie or a catheter with a special flexible tip. It is inserted through a cystoscope and used to entrap and remove stones from the ureter. Reprocessing validation data for this device type must be included in a 510(k) submission. (70 FR 56911, available at...". As of , FDA records hold no 510(k) clearances under this code and no recalls.
Classification record
- Product code
- NQT
- Device name
- Dislodger, Stone, Flexible, Ureteral, Reprocessed
- FDA definition
- A ureteral stone dislodger is a device that consists of a bougie or a catheter with a special flexible tip. It is inserted through a cystoscope and used to entrap and remove stones from the ureter. Reprocessing validation data for this device type must be included in a 510(k) submission. (70 FR 56911, available at https://www.govinfo.gov/content/pkg/FR-2005-09-29/pdf/05-19510.pdf).
- Regulation
- 21 CFR 876.4680
- Device class
- Class II
- Review panel
- Gastroenterology, Urology
- Submission type
- 510(k)
- Implant
- No
- Life sustaining or supporting
- No
- GMP exempt
- No
- Third party review eligible
- Yes
- Ingested clearances
- 0
- Ingested recalls
- 0
Companies listing this code with FDA
Companies whose registered establishments list this codeNo registered establishment in MDM’s records lists product code NQT.
FIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.