Medical Device Manufacturer · US , Grand Rapids , MI

Ventlab, LLC

1 submissions · 1 cleared · Since 2018
1
Total
1
Cleared
0
Denied

Ventlab, LLC has 1 FDA 510(k) cleared medical devices. Based in Grand Rapids, US.

Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Anesthesiology.

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

1 devices
1–1 of 1
Filters
Filter by Specialty
All1 Anesthesiology 1