CMS600P2 B-Ultrasound Diagnostic System— 510(k) K170856
Substantially EquivalentContec Medical Systems Co.,Ltd
FDA 510(k) clearance K170856 for CMS600P2 B-Ultrasound Diagnostic System, Substantially Equivalent on 2017-11-17. Applicant: Contec Medical Systems Co.,Ltd. Device class: 2.
Clearance details
- Applicant
- Contec Medical Systems Co.,Ltd
- Product code
- Code IYO
- Device class
- Class 2
- Regulation
- 21 CFR 892.1560
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Qinhuangdao, CN
Recent devices under product code IYO
view allMore clearances from Contec Medical Systems Co.,Ltd
view all- K232893 — Pocket Fetal Doppler (CONTEC 10D), Pocket Fetal Doppler (CONTEC 10E), Pocket Fetal Doppler (CONTEC 10F)
- K232895 — B-Ultrasound Diagnostic System
- K232908 — Color Doppler Ultrasound Diagnostic System (CMS1700B), Color Doppler Ultrasound Diagnostic System (CMS1700C)
- K220245 — Pocket Fetal Doppler (Models CONTEC10C and CONTEC10CL)
- K202757 — CONTEC08A Electronic Sphygmomanometer, CONTEC08C Electronic Sphygmomanometer, ABPM50 Automatic Blood Pressure Monitor
Adverse events under product code IYO
product code IYO- Malfunction
- 3,339
- Total
- 3,339
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.