Medical Device Manufacturer · US , Chicago , IL

Gibeck Respiration - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1987

Total

Cleared

Denied

Gibeck Respiration has 6 FDA 510(k) cleared medical devices. Based in Chicago, US.

Historical record: 6 cleared submissions from 1987 to 1988. Primary specialty: Anesthesiology.

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

FDA 510(k) Regulatory Record - Gibeck Respiration

6 devices

1-6 of 6