JKH Stimulator Plus— 510(k) K191151
Substantially EquivalentJkh USA, LLC
FDA 510(k) clearance K191151 for JKH Stimulator Plus, Substantially Equivalent on 2019-06-21. Applicant: Jkh USA, LLC. Device class: 2.
Clearance details
- Applicant
- Jkh USA, LLC
- Product code
- Code NUH
- Device class
- Class 2
- Regulation
- 21 CFR 882.5890
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Diamond Bar, CA, US
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More clearances from Jkh USA, LLC
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- K203635 — Patient Monitoring Cables
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- K202851 — Spo2 Sensor
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Data sourced from openFDA. This site is unofficial and independent of the FDA.