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FDA 510(k)

DeepContour (V1.0)

K-Number: K232928 · 2024-05-07

ApplicantWisdom Technologies., Inc.
Decision Date2024-05-07
Product CodeQKB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DeepContour (V1.0) is a medical device manufactured by Wisdom Technologies., Inc.. It received FDA 510(k) clearance on 2024-05-07 under approval number K232928. The device is classified under product code QKB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DeepContour (V1.0)?

DeepContour (V1.0) is a medical device that received FDA 510(k) clearance on 2024-05-07. It is manufactured by Wisdom Technologies., Inc.. The 510(k) number is K232928.

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

DeepContour (V1.0) received FDA 510(k) clearance on 2024-05-07, under approval number K232928.

What company makes DeepContour (V1.0)?

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

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

The FDA product code for DeepContour (V1.0) is QKB.

Other Devices by Wisdom Technologies., Inc.

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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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