PeekMed
K-Number: K182464 · 2018-10-25
ApplicantPeek Health, S.A.
Decision Date2018-10-25
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
PeekMed is a medical device manufactured by Peek Health, S.A.. It received FDA 510(k) clearance on 2018-10-25 under approval number K182464. 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?
PeekMed is a medical device that received FDA 510(k) clearance on 2018-10-25. It is manufactured by Peek Health, S.A.. The 510(k) number is K182464.
When was PeekMed approved by the FDA?
PeekMed received FDA 510(k) clearance on 2018-10-25, under approval number K182464.
What company makes PeekMed?
PeekMed is manufactured by Peek Health, S.A..
What is the FDA product code for PeekMed?
The FDA product code for PeekMed 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.