FORA MD6 Uric Acid Monitoring System, FORA MD6 Pro Uric Acid Monitoring System
K-Number: K181675 · 2018-12-10
Device Summary
Frequently Asked Questions
What is the FORA MD6 Uric Acid Monitoring System, FORA MD6 Pro Uric Acid Monitoring System?
FORA MD6 Uric Acid Monitoring System, FORA MD6 Pro Uric Acid Monitoring System is a medical device that received FDA 510(k) clearance on 2018-12-10. It is manufactured by Taidoc Technology Corporation. The 510(k) number is K181675.
When was FORA MD6 Uric Acid Monitoring System, FORA MD6 Pro Uric Acid Monitoring System approved by the FDA?
FORA MD6 Uric Acid Monitoring System, FORA MD6 Pro Uric Acid Monitoring System received FDA 510(k) clearance on 2018-12-10, under approval number K181675.
What company makes FORA MD6 Uric Acid Monitoring System, FORA MD6 Pro Uric Acid Monitoring System?
FORA MD6 Uric Acid Monitoring System, FORA MD6 Pro Uric Acid Monitoring System is manufactured by Taidoc Technology Corporation.
What is the FDA product code for FORA MD6 Uric Acid Monitoring System, FORA MD6 Pro Uric Acid Monitoring System?
The FDA product code for FORA MD6 Uric Acid Monitoring System, FORA MD6 Pro Uric Acid Monitoring System is PTC.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.