FORA MD6 Uric Acid Monitoring System, FORA MD6 Pro Uric Acid Monitoring System— 510(k) K181675

Substantially Equivalent

Taidoc 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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