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FDA 510(k)

ArcherQA (V1.0)

K-Number: K231273 · 2024-01-05

ApplicantWisdom Technologies., Inc.
Decision Date2024-01-05
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ArcherQA (V1.0) is a medical device manufactured by Wisdom Technologies., Inc.. It received FDA 510(k) clearance on 2024-01-05 under approval number K231273. 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 ArcherQA (V1.0)?

ArcherQA (V1.0) is a medical device that received FDA 510(k) clearance on 2024-01-05. It is manufactured by Wisdom Technologies., Inc.. The 510(k) number is K231273.

When was ArcherQA (V1.0) approved by the FDA?

ArcherQA (V1.0) received FDA 510(k) clearance on 2024-01-05, under approval number K231273.

What company makes ArcherQA (V1.0)?

ArcherQA (V1.0) is manufactured by Wisdom Technologies., Inc..

What is the FDA product code for ArcherQA (V1.0)?

The FDA product code for ArcherQA (V1.0) is IYE.

Other Devices by Wisdom Technologies., Inc.

K232928DeepContour (V1.0)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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