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FDA 510(k)

ThinkQA (Edition 2)

K-Number: K231573 · 2024-01-18

ApplicantDosisoft SA
Decision Date2024-01-18
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ThinkQA (Edition 2) is a medical device manufactured by Dosisoft SA. It received FDA 510(k) clearance on 2024-01-18 under approval number K231573. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ThinkQA (Edition 2)?

ThinkQA (Edition 2) is a medical device that received FDA 510(k) clearance on 2024-01-18. It is manufactured by Dosisoft SA. The 510(k) number is K231573.

When was ThinkQA (Edition 2) approved by the FDA?

ThinkQA (Edition 2) received FDA 510(k) clearance on 2024-01-18, under approval number K231573.

What company makes ThinkQA (Edition 2)?

ThinkQA (Edition 2) is manufactured by Dosisoft SA.

What is the FDA product code for ThinkQA (Edition 2)?

The FDA product code for ThinkQA (Edition 2) is IYE.

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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.

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