Vickers America Medical Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
22
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K840823TREONIC C30March 23, 1984
K831838LABORATORY DATA MGMT SYSTEM SDMSJanuary 24, 1984
K830748RESUSCITAIREJune 22, 1983
K830936TREONIC IP5April 12, 1983
K813239OXYGENAIRE NURING INCUBATORJanuary 28, 1982
K813238NEOCARE BABY-CONTROLLED INCUBATORJanuary 22, 1982
K811865VMA PEDIATRIC APNEA MATTRESSJuly 31, 1981
K810792NEOCARE TEMPERATURE MONITORApril 29, 1981
K810067140 NEOCARE AIR CONTROLLED INCUBATORMarch 11, 1981
K810571NEOCARE OXYGEN MONITORMarch 11, 1981
K802251SP 120 SOPHISTICATEOctober 23, 1980
K801246OXFORD HUMAN MILK PASTEURISEROctober 3, 1980
K791645VICKERS MEDICAL MODEL 112 TREONIC DC2October 2, 1979
K791713VICKERS MEDICAL MODEL 130 NEAVENT-NEOSeptember 19, 1979
K790936MODEL 114 TREONIC H150 HAEMOHEATERSeptember 4, 1979
K790657STRETCHER TRANSIT ISOLATER #122July 3, 1979
K790658AIRCRAFT TRANSIT ISOLATOR MODEL 121July 3, 1979
K790945MODEL 113 TREONIC IP3 DIGITAL SYRINGE PUJune 1, 1979
K790689REVISED BATTERY CHARGERMay 29, 1979
K781562HEMACHECKNovember 15, 1978