K260051
- 510(k) number
- K260051
- Device name
- CorVision® (91-205-Z0014)
- Applicant
- CorVent® Medical, Inc. ND · US
- Product code
- MOD — Accessory To Continuous Ventilator (Respirator)
- Decision date
- 2026-05-12
- Date received
- 2026-01-08
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Anesthesiology
PDFDownload 510(k) SummaryArchived here · 1.4 MB · U.S. public domain
Also available from FDA: K260051.pdf
Official FDA record: K260051
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.