Vickers America Medical Corp.

FDA Regulatory Profile

Vickers America Medical Corp. appears in FDA public data with 0 recalls, 22 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Mar 23, 1984.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K840823TREONIC C30Mar 23, 1984
K831838LABORATORY DATA MGMT SYSTEM SDMSJan 24, 1984
K830748RESUSCITAIREJun 22, 1983
K830936TREONIC IP5Apr 12, 1983
K813239OXYGENAIRE NURING INCUBATORJan 28, 1982
K813238NEOCARE BABY-CONTROLLED INCUBATORJan 22, 1982
K811865VMA PEDIATRIC APNEA MATTRESSJul 31, 1981
K810792NEOCARE TEMPERATURE MONITORApr 29, 1981
K810571NEOCARE OXYGEN MONITORMar 11, 1981
K810067140 NEOCARE AIR CONTROLLED INCUBATORMar 11, 1981
K802251SP 120 SOPHISTICATEOct 23, 1980
K801246OXFORD HUMAN MILK PASTEURISEROct 3, 1980
K791645VICKERS MEDICAL MODEL 112 TREONIC DC2Oct 2, 1979
K791713VICKERS MEDICAL MODEL 130 NEAVENT-NEOSep 19, 1979
K790936MODEL 114 TREONIC H150 HAEMOHEATERSep 4, 1979
K790658AIRCRAFT TRANSIT ISOLATOR MODEL 121Jul 3, 1979
K790657STRETCHER TRANSIT ISOLATER #122Jul 3, 1979
K790945MODEL 113 TREONIC IP3 DIGITAL SYRINGE PUJun 1, 1979
K790689REVISED BATTERY CHARGERMay 29, 1979
K781562HEMACHECKNov 15, 1978