PeekMed web (v1)
K-Number: K222767 · 2022-12-30
ApplicantPeek Health, S.A.
Decision Date2022-12-30
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
PeekMed web (v1) is a medical device manufactured by Peek Health, S.A.. It received FDA 510(k) clearance on 2022-12-30 under approval number K222767. 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 (v1)?
PeekMed web (v1) is a medical device that received FDA 510(k) clearance on 2022-12-30. It is manufactured by Peek Health, S.A.. The 510(k) number is K222767.
When was PeekMed web (v1) approved by the FDA?
PeekMed web (v1) received FDA 510(k) clearance on 2022-12-30, under approval number K222767.
What company makes PeekMed web (v1)?
PeekMed web (v1) is manufactured by Peek Health, S.A..
What is the FDA product code for PeekMed web (v1)?
The FDA product code for PeekMed web (v1) 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.