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FDA 510(k)

TechLive

K-Number: K243703 · 2025-06-05

ApplicantDeepHealth, Inc.
Decision Date2025-06-05
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TechLive is a medical device manufactured by DeepHealth, Inc.. It received FDA 510(k) clearance on 2025-06-05 under approval number K243703. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TechLive?

TechLive is a medical device that received FDA 510(k) clearance on 2025-06-05. It is manufactured by DeepHealth, Inc.. The 510(k) number is K243703.

When was TechLive approved by the FDA?

TechLive received FDA 510(k) clearance on 2025-06-05, under approval number K243703.

What company makes TechLive?

TechLive is manufactured by DeepHealth, Inc..

What is the FDA product code for TechLive?

The FDA product code for TechLive is LLZ.

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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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