Pocket Fetal Doppler (CONTEC 10D), Pocket Fetal Doppler (CONTEC 10E), Pocket Fetal Doppler (CONTEC 10F)— 510(k) K232893
Substantially EquivalentContec Medical Systems Co.,Ltd
FDA 510(k) clearance K232893 for Pocket Fetal Doppler (CONTEC 10D), Pocket Fetal Doppler (CONTEC 10E), Pocket Fetal Doppler (CONTEC 10F), Substantially Equivalent on 2024-06-14. Applicant: Contec Medical Systems Co.,Ltd. Device class: 2.
Clearance details
- Applicant
- Contec Medical Systems Co.,Ltd
- Product code
- Code KNG
- Device class
- Class 2
- Regulation
- 21 CFR 884.2660
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Qinhuangdao, CN
Recent devices under product code KNG
view allMore clearances from Contec Medical Systems Co.,Ltd
view all- K232895 — B-Ultrasound Diagnostic System
- K232908 — Color Doppler Ultrasound Diagnostic System (CMS1700B), Color Doppler Ultrasound Diagnostic System (CMS1700C)
- K202757 — CONTEC08A Electronic Sphygmomanometer, CONTEC08C Electronic Sphygmomanometer, ABPM50 Automatic Blood Pressure Monitor
- K201980 — Infrared Thermometer
- K171360 — CONTEC Electrocardiograph
Data sourced from openFDA. This site is unofficial and independent of the FDA.