Medical Device Manufacturer · US , Walker , MI

Artec Environmental Monitoring Division - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1983

7

Total

7

Cleared

0

Denied

FDA 510(k) Regulatory Record - Artec Environmental Monitoring Division Anesthesiology ✕

6 devices

1-6 of 6

Cleared Feb 06, 1990

ARTEC RESPOND PULMONARY RESUSCITATOR

Anesthesiology · 60d

Cleared Sep 28, 1987

MOUTH TO FACE RESUSCITATOR

Anesthesiology · 55d

Cleared Oct 20, 1986

Anesthesiology · 12d

Cleared Jan 03, 1986

ANESTHESIA SHUTOFF VALVE POSITIVE CLOSURE

Anesthesiology · 50d

Cleared Jan 17, 1984

Anesthesiology · 174d

Cleared Mar 09, 1983

ARTEC TWIST VALVE

Anesthesiology · 62d