PeekMed web
K-Number: K240926 · 2024-12-06
ApplicantPeek Health, S.A.
Decision Date2024-12-06
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
PeekMed web is a medical device manufactured by Peek Health, S.A.. It received FDA 510(k) clearance on 2024-12-06 under approval 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. It is manufactured by Peek Health, S.A.. The 510(k) number is K240926.
When was PeekMed web approved by the FDA?
PeekMed web received FDA 510(k) clearance on 2024-12-06, under approval number K240926.
What company makes PeekMed web?
PeekMed web is manufactured by Peek Health, S.A..
What is the FDA product code for PeekMed web?
The FDA product code for PeekMed web is LLZ.
Other Devices by Peek Health, S.A.
Related Devices (Code: LLZ)
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.