Shenzhen Wisonic Medical Technology Co. , Ltd.
Shenzhen Wisonic Medical Technology Co. , Ltd. appears in FDA public data with 0 recalls, 7 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Sep 15, 2023.
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Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 0
- Compliance Actions
- 0
Known Names
Shenzhen Wisonic Medical Technology Co, Shenzhen Wisonic Medical Technology Co.
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K230066 | Carnation series Diagnostic Ultrasound System | Sep 15, 2023 |
| K211886 | Clivia series Diagnostic Ultrasound System | Dec 2, 2021 |
| K210154 | Labat series Diagnostic Ultrasound System | Jul 30, 2021 |
| K191347 | Paragon XHD Diagnostic Ultrasound System | Feb 7, 2020 |
| K182715 | Piloter Exp/Piloter/Piloter P Diagnostic Ultrasound System | Nov 20, 2018 |
| K180461 | Navi e/Navi s/Navi X Diagnostic Ultrasound System | May 9, 2018 |
| K163712 | Clover 50/Clover60/Clover70 Diagnostic Ultrasound System | Jan 2, 2018 |