K230889
- 510(k) number
- K230889
- Device name
- Digital Thermometer
- Applicant
- Wenzhou Yosun Medical Technology Co.,Ltd CN
- Product code
- FLL — Continuous Measurement Thermometer
- Decision date
- 2024-04-03
- Date received
- 2023-03-31
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General Hospital
This submission filed a 510(k) Statement rather than a Summary; no public summary is available from FDA.
Official FDA record: K230889
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.