Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Norwich Eaton Pharmaceuticals, Inc.

FDA 510(k) & PMA Approved Devices — 10 products

Total Devices10
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K842841 VIVONEX TUNG STEN TIP TUBEKNT1984-08-14 View
510(k) K831968 VIVONEX TUNGSTEN TIP TUBE-BRAIDEDKNT1983-09-01 View
510(k) K831969 VIVONEX TUNGSTEN TIP TUBE-WOUNDKNT1983-09-01 View
510(k) K831971 VIVONEX TUNGSTEN TIP TUBE-TWISTED WIREKNT1983-09-01 View
510(k) K831970 VIVONEX TUNGSTEN TIP TUBE-MONOFILA-KNT1983-07-18 View
510(k) K822516 VIVONEX MASS GASTRASTOMY TUBEKHT1982-09-07 View
510(k) K821231 VIVONEX TUNGSTEN TIP TUBE PLACEMENTKNT1982-05-10 View
510(k) K821067 VIVONEX ACUTROL ENTERNAL FEEDING SYSKNT1982-04-29 View
510(k) K811968 VIVONEX TUNGSTEN TIPKNT1981-08-25 View
510(k) K802300 VIVONEX JEJUNOSTOMY KITKNT1980-10-23 View
↑