Incontinence Probe— 510(k) K210441
Substantially EquivalentShenzhen Med-Link Electronics Tech Co., Ltd.
FDA 510(k) clearance K210441 for Incontinence Probe, Substantially Equivalent on 2021-09-17. Applicant: Shenzhen Med-Link Electronics Tech Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Shenzhen Med-Link Electronics Tech Co., Ltd.
- Product code
- Code KPI
- Device class
- Class 2
- Regulation
- 21 CFR 876.5320
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Shenzhen, CN
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More clearances from Shenzhen Med-Link Electronics Tech Co., Ltd.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.