FDA 510(k)

NEURO N100 RADIOFREQUENCY GENERATOR AND ACCESSORY CABLES

K-Number: K010969 · 2001-04-20

Decision Date2001-04-20

Product CodeGXD

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

NEURO N100 RADIOFREQUENCY GENERATOR AND ACCESSORY CABLES is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Instruments. It received FDA 510(k) clearance on 2001-04-20 under 510(k) number K010969. The device is classified under product code GXD. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEURO N100 RADIOFREQUENCY GENERATOR AND ACCESSORY CABLES?

NEURO N100 RADIOFREQUENCY GENERATOR AND ACCESSORY CABLES is a medical device that received FDA 510(k) clearance on 2001-04-20. The listed applicant is Stryker Instruments. The 510(k) number is K010969.

When did NEURO N100 RADIOFREQUENCY GENERATOR AND ACCESSORY CABLES receive FDA 510(k) clearance?

NEURO N100 RADIOFREQUENCY GENERATOR AND ACCESSORY CABLES received FDA 510(k) clearance on 2001-04-20, under 510(k) number K010969.

Who is the listed applicant for NEURO N100 RADIOFREQUENCY GENERATOR AND ACCESSORY CABLES?

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

What is the FDA product code for NEURO N100 RADIOFREQUENCY GENERATOR AND ACCESSORY CABLES?

The FDA product code for NEURO N100 RADIOFREQUENCY GENERATOR AND ACCESSORY CABLES is GXD.

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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.