Medical Device Manufacturer · US , Walker , MI

Oeco - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1981
2
Total
2
Cleared
0
Denied

Oeco has 2 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 2 cleared submissions from 1981 to 1981. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Oeco Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Oeco

2 devices
1-2 of 2
Cleared Jul 31, 1981
OECO APNEA MONITOR
K811628 · BZQ
Anesthesiology · 52d
Cleared Jul 02, 1981
OECO NASAL CANNULA
K811789 · CAT
Anesthesiology · 8d
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