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FDA 510(k)

MICRO-RECORDING AND STIMULATION ELECTRODES-MICRO MACROELECTRODE MODEL NO. 230700-230799

K-Number: K041409 · 2004-08-20

ApplicantInomed GmbH
Decision Date2004-08-20
Product CodeGZL
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MICRO-RECORDING AND STIMULATION ELECTRODES-MICRO MACROELECTRODE MODEL NO. 230700-230799 is the device name listed in this FDA 510(k) record. The listed applicant is Inomed GmbH. It received FDA 510(k) clearance on 2004-08-20 under 510(k) number K041409. The device is classified under product code GZL. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRO-RECORDING AND STIMULATION ELECTRODES-MICRO MACROELECTRODE MODEL NO. 230700-230799?

MICRO-RECORDING AND STIMULATION ELECTRODES-MICRO MACROELECTRODE MODEL NO. 230700-230799 is a medical device that received FDA 510(k) clearance on 2004-08-20. The listed applicant is Inomed GmbH. The 510(k) number is K041409.

When did MICRO-RECORDING AND STIMULATION ELECTRODES-MICRO MACROELECTRODE MODEL NO. 230700-230799 receive FDA 510(k) clearance?

MICRO-RECORDING AND STIMULATION ELECTRODES-MICRO MACROELECTRODE MODEL NO. 230700-230799 received FDA 510(k) clearance on 2004-08-20, under 510(k) number K041409.

Who is the listed applicant for MICRO-RECORDING AND STIMULATION ELECTRODES-MICRO MACROELECTRODE MODEL NO. 230700-230799?

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

What is the FDA product code for MICRO-RECORDING AND STIMULATION ELECTRODES-MICRO MACROELECTRODE MODEL NO. 230700-230799?

The FDA product code for MICRO-RECORDING AND STIMULATION ELECTRODES-MICRO MACROELECTRODE MODEL NO. 230700-230799 is GZL.

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Related Devices (Code: GZL)

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Official Source

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