Norwich Eaton Pharmaceuticals, Inc.
Norwich Eaton Pharmaceuticals, Inc. holds FDA 510(k) medical device clearances, first cleared 1980, most recent 1984.
Top product codes for Norwich Eaton Pharmaceuticals, Inc.
Recent clearances by Norwich Eaton Pharmaceuticals, Inc.
- K842841 — VIVONEX TUNG STEN TIP TUBE
- K831968 — VIVONEX TUNGSTEN TIP TUBE-BRAIDED
- K831969 — VIVONEX TUNGSTEN TIP TUBE-WOUND
- K831971 — VIVONEX TUNGSTEN TIP TUBE-TWISTED WIRE
- K831970 — VIVONEX TUNGSTEN TIP TUBE-MONOFILA-
- K822516 — VIVONEX MASS GASTRASTOMY TUBE
- K821231 — VIVONEX TUNGSTEN TIP TUBE PLACEMENT
- K821067 — VIVONEX ACUTROL ENTERNAL FEEDING SYS
- K811968 — VIVONEX TUNGSTEN TIP
- K802300 — VIVONEX JEJUNOSTOMY KIT
Data sourced from openFDA. This site is unofficial and independent of the FDA.