FORA MD6 Uric Acid Monitoring System, FORA MD6 Pro Uric Acid Monitoring System
FDA 510(k) clearance K181675 · decided 2018-12-10
Clearance details
- K-number
- K181675
- Device name
- FORA MD6 Uric Acid Monitoring System, FORA MD6 Pro Uric Acid Monitoring System
- Applicant
- Taidoc Technology Corporation
- Decision
- Substantially Equivalent
- Date received
- 2018-06-25
- Decision date
- 2018-12-10
- Days to decision
- 168 days
- Clearance type
- Traditional
- Product code
- PTC
- Device class
- 1
- Regulation number
- 862.1775
- Medical specialty
- Clinical Chemistry
- Advisory committee
- Clinical Chemistry
- Location
- New Taipei City, TW
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| UASure II Blood Uric Acid Monitoring System (K242209) | Apex BioTechnology Corp. | 2025-04-04 |
| Nova Max Uric Acid Monitoring System (K160990) | Nova Biomedical Corporation | 2017-04-11 |
Recalls involving this device
No recalls on record reference this clearance.