K241135
- 510(k) number
- K241135
- Device name
- RESPOND(R) Ventilator
- Applicant
- Corvent Medical, Inc. ND · US
- Product code
- CBK — Ventilator, Continuous, Facility Use
- Decision date
- 2024-11-13
- Date received
- 2024-04-24
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Anesthesiology
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K241135.pdf
Official FDA record: K241135
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.