Product code JCY— General, Plastic Surgery
BLOOD TRANSFUSION SET (SANGOFIX)
- Classification name
- Catheter, Infusion
- Device class
- Class 1
- Regulation
- 21 CFR 878.4200
- Advisory panel
- General, Plastic Surgery
- Total cleared
- 14
- First cleared
- Most recent
Market context for product code JCY
FDA has cleared devices under product code JCY between 1976 and 1986, filed by 10 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.
Clearances per year
- 1986
- 1984
- 1983
- 1982
- 1979
- 1977
- 1976
Top applicants under product code JCY
Recent clearances under product code JCY
- K863982 — VAS-CATH PERICARDIOCENTESIS CATHETER, SET & TRAY
- K840324 — SILICONE SUMP DRAIN 20 & 40 FRENCH
- K834615 — TRIPLE LUMEN INFUSIONCATHETERS-
- K831453 — SILCATH CENTRAL CATHETER TRAY W/18 GA
- K831451 — SILCATH CENTRAL CATHETER TRAY SIZE-
- K822096 — CHEMOTHERAPY INFUSION CATHETER
- K813606 — SILICONE ELASTOMER INFUSION CATHETER
- K791372 — JELCO & KVO CATHETER PLACEMENT UNIT
- K771861 — CATHETER, CEBTRAL VENOUS, 2N1501
- K760760 — CATHETER, INTRAVASCULAR (ARGYLE IV SK)
- K760380 — INTRAVENOUS TRANSFER SET (INTRAFIX)
- K760381 — BLOOD TRANSFUSION SET (SANGOFIX)
- K760390 — CATHETER, VEIN (BRAUNULA T)
- K760391 — CATHETER, VEIN (BRAUNULA)
Data sourced from openFDA. This site is unofficial and independent of the FDA.