NeuroCap
K-Number: K172866 · 2018-04-27
ApplicantMemory MD, Inc.
Decision Date2018-04-27
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
NeuroCap is a medical device manufactured by Memory MD, Inc.. It received FDA 510(k) clearance on 2018-04-27 under approval number K172866. The device is classified under product code GXY. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the NeuroCap?
NeuroCap is a medical device that received FDA 510(k) clearance on 2018-04-27. It is manufactured by Memory MD, Inc.. The 510(k) number is K172866.
When was NeuroCap approved by the FDA?
NeuroCap received FDA 510(k) clearance on 2018-04-27, under approval number K172866.
What company makes NeuroCap?
NeuroCap is manufactured by Memory MD, Inc..
What is the FDA product code for NeuroCap?
The FDA product code for NeuroCap is GXY.
Other Devices by Memory MD, Inc.
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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.