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FDA 510(k)

NEUROTRON 100

K-Number: K833086 · 1984-01-24

ApplicantNeutro-Tronics
Decision Date1984-01-24
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NEUROTRON 100 is the device name listed in this FDA 510(k) record. The listed applicant is Neutro-Tronics. It received FDA 510(k) clearance on 1984-01-24 under 510(k) number K833086. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEUROTRON 100?

NEUROTRON 100 is a medical device that received FDA 510(k) clearance on 1984-01-24. The listed applicant is Neutro-Tronics. The 510(k) number is K833086.

When did NEUROTRON 100 receive FDA 510(k) clearance?

NEUROTRON 100 received FDA 510(k) clearance on 1984-01-24, under 510(k) number K833086.

Who is the listed applicant for NEUROTRON 100?

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

What is the FDA product code for NEUROTRON 100?

The FDA product code for NEUROTRON 100 is GZJ.

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Related Devices (Code: GZJ)

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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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