K230423
- 510(k) number
- K230423
- Device name
- Electronic Peak Flow Meter
- Applicant
- Taian Dalu Medical Instrument Co., Ltd. CN
- Product code
- BZH — Meter, Peak Flow, Spirometry
- Decision date
- 2024-02-23
- Date received
- 2023-02-17
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Anesthesiology
510(k) Summary (official FDA PDF): K230423.pdf
Official FDA record: K230423
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.