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FDA 510(k)

PeekMed web

K-Number: K240926 · 2024-12-06

Decision Date2024-12-06
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PeekMed web is the device name listed in this FDA 510(k) record. The listed applicant is Peek Health, S.A.. It received FDA 510(k) clearance on 2024-12-06 under 510(k) number K240926. 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 PeekMed web?

PeekMed web is a medical device that received FDA 510(k) clearance on 2024-12-06. The listed applicant is Peek Health, S.A.. The 510(k) number is K240926.

When did PeekMed web receive FDA 510(k) clearance?

PeekMed web received FDA 510(k) clearance on 2024-12-06, under 510(k) number K240926.

Who is the listed applicant for PeekMed web?

The FDA 510(k) record lists Peek Health, S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PeekMed web?

The FDA product code for PeekMed web is LLZ.

Other records listing Peek Health, S.A. 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.

View all 7 devices →

Related Devices (Code: LLZ)

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.

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.