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FDA 510(k)

MODEL 8 EEG PREAMPLIFIER

K-Number: K863124 · 1986-11-18

ApplicantMicro Tronics Corp.
Decision Date1986-11-18
Product CodeGWQ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MODEL 8 EEG PREAMPLIFIER is the device name listed in this FDA 510(k) record. The listed applicant is Micro Tronics Corp.. It received FDA 510(k) clearance on 1986-11-18 under 510(k) number K863124. 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 MODEL 8 EEG PREAMPLIFIER?

MODEL 8 EEG PREAMPLIFIER is a medical device that received FDA 510(k) clearance on 1986-11-18. The listed applicant is Micro Tronics Corp.. The 510(k) number is K863124.

When did MODEL 8 EEG PREAMPLIFIER receive FDA 510(k) clearance?

MODEL 8 EEG PREAMPLIFIER received FDA 510(k) clearance on 1986-11-18, under 510(k) number K863124.

Who is the listed applicant for MODEL 8 EEG PREAMPLIFIER?

The FDA 510(k) record lists Micro Tronics Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL 8 EEG PREAMPLIFIER?

The FDA product code for MODEL 8 EEG PREAMPLIFIER is GWQ.

Related Clinical Trials

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.

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Other records listing Micro Tronics Corp. 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.

K901797THE WONDER BOXK890513SAC 747 AND SAC 847 (SLEEP ANALYZING COMPUTERS)K862527SLEEP ANALYZING COMPUTERK780838PERCIK772005MYOTONE EMG MONITOR

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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