K240375
- 510(k) number
- K240375
- Device name
- V80 Anesthetic Vaporizer (V80)
- Applicant
- Shenzhen Mindray Bio-Medical Electronics Co., Ltd. CN
- Product code
- CAD — Vaporizer, Anesthesia, Non-Heated
- Decision date
- 2024-10-31
- Date received
- 2024-02-07
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Anesthesiology
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K240375.pdf
Official FDA record: K240375
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.