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FDA 510(k)

NEURON II AND MICROTENS

K-Number: K935395 · 1994-04-15

ApplicantDatran Corp.
Decision Date1994-04-15
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NEURON II AND MICROTENS is the device name listed in this FDA 510(k) record. The listed applicant is Datran Corp.. It received FDA 510(k) clearance on 1994-04-15 under 510(k) number K935395. 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 NEURON II AND MICROTENS?

NEURON II AND MICROTENS is a medical device that received FDA 510(k) clearance on 1994-04-15. The listed applicant is Datran Corp.. The 510(k) number is K935395.

When did NEURON II AND MICROTENS receive FDA 510(k) clearance?

NEURON II AND MICROTENS received FDA 510(k) clearance on 1994-04-15, under 510(k) number K935395.

Who is the listed applicant for NEURON II AND MICROTENS?

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

What is the FDA product code for NEURON II AND MICROTENS?

The FDA product code for NEURON II AND MICROTENS is 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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