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FDA 510(k)

FORA MD6 Uric Acid Monitoring System, FORA MD6 Pro Uric Acid Monitoring System

K-Number: K181675 · 2018-12-10

Decision Date2018-12-10
Product CodePTC
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

FORA MD6 Uric Acid Monitoring System, FORA MD6 Pro Uric Acid Monitoring System is a medical device manufactured by Taidoc Technology Corporation. It received FDA 510(k) clearance on 2018-12-10 under approval number K181675. The device is classified under product code PTC. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

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

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