Product code FIQ— Gastroenterology, Urology
ARTERIO VENOUS SHUNT CANNULA & ADAPTORS
- Classification name
- Cannula, A-V Shunt
- Device class
- Class 2
- Regulation
- 21 CFR 876.5540
- Advisory panel
- Gastroenterology, Urology
- Total cleared
- 23
- First cleared
- Most recent
Market context for product code FIQ
FDA has cleared devices under product code FIQ between 1977 and 1989, filed by 12 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.
Clearances per year
- 1989
- 1985
- 1984
- 1983
- 1982
- 1981
- 1980
- 1979
- 1978
- 1977
Top applicants under product code FIQ
Recent clearances under product code FIQ
- K892887 — ST SERIES SAF-T-SHUNTS ARTERIOVENOUS CANNULA
- K892663 — S-100 ALLEN-BROWN SHUNT
- K892666 — SAF-T-SHUNT, S-300 SERIES
- K844692 — PEDIATRIC SIZED HEMOCATH CATHETER
- K841791 — PLUME FISTULA NEEDLE
- K840322 — HEMOFILTRATION CATHETER HF-100
- K840415 — HEMOCATH
- K834358 — PARALLEL DUAL LUMEN SUBCLAVIAN CANNULA
- K840436 — HEMASITE/RENALOY -VASCULAR ACCESS SHUNT
- K833622 — RENALLOY HEMASITE VASCULAR ACCESS SHUNT
- K831801 — HEMOCLAV VENOUS CATHETER
- K831401 — SINGLE NEEDLE SUBCLAVIAN VEIN ACCESS
- K831440 — SINGLE NEEDLE SUBCLAVIAN VEIN MWI250/260
- K823752 — EXTRACORPOREAL SUBCLAVIAN CATHETER KIT
- K822880 — ARTERIO VENOUS SHUNT CANNULA & ADAPTORS
- K813237 — HEMASITE VASCULAR ACCESS SHUNT HM-1000
- K812890 — HEMASITE GRAFTLESS VASCULAR ACESS
- K811384 — HEMASITE VASCULAR ACCESS SHUNT
- K810114 — VASCULAR ACCESS SYSTEM
- K801478 — SSC8 SORENSON SUBCLAVIAN CATHETER
- K791308 — ULDALL SUBCLAVIAN CANNULA SC-100
- K780484 — SILASTIC BRAND PENILE IMPLANT
- K760973 — HEMODIALYSIS CANNULA & FEMORAL CLAMP
Data sourced from openFDA. This site is unofficial and independent of the FDA.