KNZ — Accessories, A-V Shunt Class II
FDA product code KNZ covers "Accessories, A-V Shunt", a Class II medical device regulated under 21 CFR 876.5540. Submissions are reviewed by the Gastroenterology, Urology panel. Devices under this code are implants. At least 10 recent 510(k) clearances have been granted under this product code.
Classification Details
- Product Code
- KNZ
- Device Class
- Class II
- Regulation Number
- 876.5540
- Submission Type
- Review Panel
- GU
- Medical Specialty
- Gastroenterology, Urology
- Implant
- Yes
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K842039 | argon medical | ARGON DUAL LUMEN HEMODIALYSIS, CATHETER | January 29, 1985 |
| K844612 | packaging technologies | ACUTE HEMODIALYSIS TRAYS | December 17, 1984 |
| K842864 | vas-cath of canada | VACCESS FEMORAL CANNULA | August 8, 1984 |
| K842416 | medical components | DUO FLOW CATHETER-MC 54 | July 26, 1984 |
| K841530 | medical components | DOUBLE LUMEN SUBLCAVIAN-FEMORAL | June 25, 1984 |
| K841119 | top surgical manufacturers | TOPS DISPOS. INFUSION SET/HEMODIALYSIS | April 20, 1984 |
| K840424 | quinton | HEMOCATH REPAIR KIT | March 5, 1984 |
| K840437 | renal systems | HEMASITE ACCESSORIES MODIFICATION | February 21, 1984 |
| K834510 | renal systems | RENAFLO AVF SET FOR HEMODIALYSIS | February 4, 1984 |
| K833139 | intermed | ACUTE HEMODIALYSIS TRAYS | December 22, 1983 |