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FDA 510(k)

DIGITAL ELECTRONEUROMETER S-100

K-Number: K843924 · 1985-03-12

ApplicantNeurotron, Inc.
Decision Date1985-03-12
Product CodeJXE
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

DIGITAL ELECTRONEUROMETER S-100 is the device name listed in this FDA 510(k) record. The listed applicant is Neurotron, Inc.. It received FDA 510(k) clearance on 1985-03-12 under 510(k) number K843924. The device is classified under product code JXE. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIGITAL ELECTRONEUROMETER S-100?

DIGITAL ELECTRONEUROMETER S-100 is a medical device that received FDA 510(k) clearance on 1985-03-12. The listed applicant is Neurotron, Inc.. The 510(k) number is K843924.

When did DIGITAL ELECTRONEUROMETER S-100 receive FDA 510(k) clearance?

DIGITAL ELECTRONEUROMETER S-100 received FDA 510(k) clearance on 1985-03-12, under 510(k) number K843924.

Who is the listed applicant for DIGITAL ELECTRONEUROMETER S-100?

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

What is the FDA product code for DIGITAL ELECTRONEUROMETER S-100?

The FDA product code for DIGITAL ELECTRONEUROMETER S-100 is JXE.

Related Clinical Trials

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Other records listing Neurotron, 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.

K853608NEUROMETER

Related Devices (Code: JXE)

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.

K240189NM-01/CPT neurometer (NM-01/CPT)Mde Orvosbiológiai Kutató, Fejleszto,K190536Mediracer NCSMediracer OYK070109NEUROMETRIX ADVANCENeurometrix, Inc.K060584NC-STATNeurometrix, Inc.K053058XLTEK NEUROPATH, MODEL PK1070Excel Tech. , Ltd.K052904VIRTUAL MEDICAL SYSTEMS MODEL VT3000Scientific Imaging, 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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