K233823
- 510(k) number
- K233823
- Device name
- Ultrasonic Fetal Doppler
- Applicant
- Shenzhen Jamr Technology Co., Ltd. CN
- Product code
- KNG — Monitor, Ultrasonic, Fetal
- Decision date
- 2024-06-28
- Date received
- 2023-12-01
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Obstetrics/Gynecology
This submission filed a 510(k) Statement rather than a Summary; no public summary is available from FDA.
Official FDA record: K233823
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.