FORA MD6 Uric Acid Monitoring System, FORA MD6 Pro Uric Acid Monitoring System— 510(k) K181675
Substantially EquivalentTaidoc Technology Corporation
FDA 510(k) clearance K181675 for FORA MD6 Uric Acid Monitoring System, FORA MD6 Pro Uric Acid Monitoring System, Substantially Equivalent on 2018-12-10. Applicant: Taidoc Technology Corporation. Device class: 1.
Clearance details
- Applicant
- Taidoc Technology Corporation
- Product code
- Code PTC
- Device class
- Class 1
- Regulation
- 21 CFR 862.1775
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- New Taipei City, TW
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Data sourced from openFDA. This site is unofficial and independent of the FDA.