FDA 510(k)

TechLive

K-Number: K243703 · 2025-06-05

Decision Date2025-06-05

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

TechLive is the device name listed in this FDA 510(k) record. The listed applicant is DeepHealth, Inc.. It received FDA 510(k) clearance on 2025-06-05 under 510(k) 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. The listed applicant is DeepHealth, Inc.. The 510(k) number is K243703.

When did TechLive receive FDA 510(k) clearance?

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

Who is the listed applicant for TechLive?

The FDA 510(k) record lists DeepHealth, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TechLive?

The FDA product code for TechLive is LLZ.

Other records listing DeepHealth, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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.