KQQ — Tubing, Dialysate (And Connector) Class II
FDA product code KQQ covers "Tubing, Dialysate (And Connector)", a Class II medical device regulated under 21 CFR 876.5820. Submissions are reviewed by the Gastroenterology, Urology panel. At least 1 recent 510(k) clearance has been granted under this product code.
Classification Details
- Product Code
- KQQ
- Device Class
- Class II
- Regulation Number
- 876.5820
- Submission Type
- Review Panel
- GU
- Medical Specialty
- Gastroenterology, Urology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K830811 | steridoc | ASEPTIC FLUID TRANSFER SYSTEM | April 28, 1983 |