Medical Device Manufacturer · SE , Sweden

Artema Medical AB - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1991

5

Total

5

Cleared

0

Denied

FDA 510(k) Regulatory Record - Artema Medical AB Anesthesiology ✕

5 devices

1-5 of 5

Cleared Feb 21, 1995

AQUA+I-F, I-H, I-FH, II-H, II-FH, III-H

Anesthesiology · 111d

Cleared Jul 26, 1991

Anesthesiology · 63d

Cleared Jul 26, 1991

ARTEMA AQUA+ T & TS

Anesthesiology · 63d

Cleared Jul 26, 1991

Anesthesiology · 63d

Cleared Jul 26, 1991

ARTEMA AQUA+ FLEX

Anesthesiology · 63d