XPER Technology PREMIUM Pro Blood Glucose Monitoring System— 510(k) K221349
Substantially EquivalentTaidoc Technology Corporation
FDA 510(k) clearance K221349 for XPER Technology PREMIUM Pro Blood Glucose Monitoring System, Substantially Equivalent on 2024-11-19. Applicant: Taidoc Technology Corporation. Device class: 2.
Clearance details
- Applicant
- Taidoc Technology Corporation
- Product code
- Code PZI
- Device class
- Class 2
- Regulation
- 21 CFR 862.1345
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Dual Track
- Location
- New Taipei City, TW
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Data sourced from openFDA. This site is unofficial and independent of the FDA.