NEUROShield
K-Number: K220034 · 2023-09-14
ApplicantIn-Med Prognostics L3c
Decision Date2023-09-14
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
NEUROShield is a medical device manufactured by In-Med Prognostics L3c. It received FDA 510(k) clearance on 2023-09-14 under approval number K220034. 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 NEUROShield?
NEUROShield is a medical device that received FDA 510(k) clearance on 2023-09-14. It is manufactured by In-Med Prognostics L3c. The 510(k) number is K220034.
When was NEUROShield approved by the FDA?
NEUROShield received FDA 510(k) clearance on 2023-09-14, under approval number K220034.
What company makes NEUROShield?
NEUROShield is manufactured by In-Med Prognostics L3c.
What is the FDA product code for NEUROShield?
The FDA product code for NEUROShield is LLZ.
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.