AccuPoint Electrode
K-Number: K162459 · 2017-06-15
Decision Date2017-06-15
Product CodeGZL
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
AccuPoint Electrode is a medical device manufactured by Microprobes For Life Science, Inc. Dba Neuron. It received FDA 510(k) clearance on 2017-06-15 under approval number K162459. The device is classified under product code GZL. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the AccuPoint Electrode?
AccuPoint Electrode is a medical device that received FDA 510(k) clearance on 2017-06-15. It is manufactured by Microprobes For Life Science, Inc. Dba Neuron. The 510(k) number is K162459.
When was AccuPoint Electrode approved by the FDA?
AccuPoint Electrode received FDA 510(k) clearance on 2017-06-15, under approval number K162459.
What company makes AccuPoint Electrode?
AccuPoint Electrode is manufactured by Microprobes For Life Science, Inc. Dba Neuron.
What is the FDA product code for AccuPoint Electrode?
The FDA product code for AccuPoint Electrode is GZL.
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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.