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Artema Medical AB

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K945359AQUA+I-F, I-H, I-FH, II-H, II-FH, III-HFebruary 21, 1995
K912336ARTEMA AQUA+ FLEXJuly 26, 1991
K912334ARTEMA AQUA+ T & TSJuly 26, 1991
K912335ARTEMA AQUA+ NJuly 26, 1991
K912333ARTEMA AQUA+July 26, 1991