NeuroCap (Model DEC22)
K-Number: K202913 · 2021-03-05
ApplicantMemory MD, Inc.
Decision Date2021-03-05
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
NeuroCap (Model DEC22) is a medical device manufactured by Memory MD, Inc.. It received FDA 510(k) clearance on 2021-03-05 under approval number K202913. 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 (Model DEC22)?
NeuroCap (Model DEC22) is a medical device that received FDA 510(k) clearance on 2021-03-05. It is manufactured by Memory MD, Inc.. The 510(k) number is K202913.
When was NeuroCap (Model DEC22) approved by the FDA?
NeuroCap (Model DEC22) received FDA 510(k) clearance on 2021-03-05, under approval number K202913.
What company makes NeuroCap (Model DEC22)?
NeuroCap (Model DEC22) is manufactured by Memory MD, Inc..
What is the FDA product code for NeuroCap (Model DEC22)?
The FDA product code for NeuroCap (Model DEC22) is GXY.
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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.