Artec Environmental Monitoring Division

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K900839THE CAROLINA ROCKERApril 18, 1990
K896886ARTEC RESPOND PULMONARY RESUSCITATORFebruary 6, 1990
K873043MOUTH TO FACE RESUSCITATORSeptember 28, 1987
K863910RAINCOATOctober 20, 1986
K854573ANESTHESIA SHUTOFF VALVE POSITIVE CLOSUREJanuary 3, 1986
K832512AIRWAY MASKSJanuary 17, 1984
K830056ARTEC TWIST VALVEMarch 9, 1983