Medical Device Manufacturer · US , Mchenry , IL

Dytek Corp. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1976

3

Total

3

Cleared

0

Denied

FDA 510(k) Regulatory Record - Dytek Corp. Anesthesiology ✕

2 devices

1-2 of 2

Cleared Sep 20, 1978

LUNG EXER. BAG, POST-OP, MODIFIED

Anesthesiology · 65d

Cleared Aug 06, 1976

BAG, POST OPERATIVE LUNG EXERCIZING BLOW

Anesthesiology · 31d