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FDA 510(k)

E*NET NEUROMONITORING SYSTEM

K-Number: K930080 · 1993-10-19

ApplicantPhysiometrix, Inc.
Decision Date1993-10-19
Product CodeGWQ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

E*NET NEUROMONITORING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Physiometrix, Inc.. It received FDA 510(k) clearance on 1993-10-19 under 510(k) number K930080. 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 E*NET NEUROMONITORING SYSTEM?

E*NET NEUROMONITORING SYSTEM is a medical device that received FDA 510(k) clearance on 1993-10-19. The listed applicant is Physiometrix, Inc.. The 510(k) number is K930080.

When did E*NET NEUROMONITORING SYSTEM receive FDA 510(k) clearance?

E*NET NEUROMONITORING SYSTEM received FDA 510(k) clearance on 1993-10-19, under 510(k) number K930080.

Who is the listed applicant for E*NET NEUROMONITORING SYSTEM?

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

What is the FDA product code for E*NET NEUROMONITORING SYSTEM?

The FDA product code for E*NET NEUROMONITORING SYSTEM is GWQ.

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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

View on FDA Database →

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

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