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FDA 510(k)

NEUROMAPPER 1620

K-Number: K870263 · 1987-04-10

ApplicantNeuroscience, Inc.
Decision Date1987-04-10
Product CodeGWQ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NEUROMAPPER 1620 is the device name listed in this FDA 510(k) record. The listed applicant is Neuroscience, Inc.. It received FDA 510(k) clearance on 1987-04-10 under 510(k) number K870263. The device is classified under product code GWQ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEUROMAPPER 1620?

NEUROMAPPER 1620 is a medical device that received FDA 510(k) clearance on 1987-04-10. The listed applicant is Neuroscience, Inc.. The 510(k) number is K870263.

When did NEUROMAPPER 1620 receive FDA 510(k) clearance?

NEUROMAPPER 1620 received FDA 510(k) clearance on 1987-04-10, under 510(k) number K870263.

Who is the listed applicant for NEUROMAPPER 1620?

The FDA 510(k) record lists Neuroscience, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEUROMAPPER 1620?

The FDA product code for NEUROMAPPER 1620 is GWQ.

Related Clinical Trials

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Other records listing Neuroscience, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K871931ISTAT SOFTWAREK855232SOMATOSENSORY EVOKED POTENTIAL STIMULATORK850430NEUROSCIENCE MAP-10 EEG

Related Devices (Code: GWQ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261604Enobio Dx (Enobio Dx 8);Enobio Dx (Enobio Dx 20);Enobio Dx (Enobio Dx 32)Neuroelectrics Barcelona S.L.U.K260455New Wave SystemZeto, Inc.K233403Flexset SystemZeto, Inc.K231366Neuronaute PlusBioserenity SasK221959Q21Neurofield, Inc.K231457SPARK ScanSpark Neuro, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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