Norwich Eaton Pharmaceuticals, Inc.
Norwich Eaton Pharmaceuticals, Inc. appears in FDA public data with 0 recalls, 10 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on August 14, 1984.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 10
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K842841 | VIVONEX TUNG STEN TIP TUBE | August 14, 1984 |
| K831969 | VIVONEX TUNGSTEN TIP TUBE-WOUND | September 1, 1983 |
| K831968 | VIVONEX TUNGSTEN TIP TUBE-BRAIDED | September 1, 1983 |
| K831971 | VIVONEX TUNGSTEN TIP TUBE-TWISTED WIRE | September 1, 1983 |
| K831970 | VIVONEX TUNGSTEN TIP TUBE-MONOFILA- | July 18, 1983 |
| K822516 | VIVONEX MASS GASTRASTOMY TUBE | September 7, 1982 |
| K821231 | VIVONEX TUNGSTEN TIP TUBE PLACEMENT | May 10, 1982 |
| K821067 | VIVONEX ACUTROL ENTERNAL FEEDING SYS | April 29, 1982 |
| K811968 | VIVONEX TUNGSTEN TIP | August 25, 1981 |
| K802300 | VIVONEX JEJUNOSTOMY KIT | October 23, 1980 |