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FDA 510(k)

MAVIDON MEDICAL ELECTRODE JELLY

K-Number: K003924 · 2001-08-24

ApplicantMavidon Medical Products
Decision Date2001-08-24
Product CodeGYB
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MAVIDON MEDICAL ELECTRODE JELLY is the device name listed in this FDA 510(k) record. The listed applicant is Mavidon Medical Products. It received FDA 510(k) clearance on 2001-08-24 under 510(k) number K003924. The device is classified under product code GYB. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAVIDON MEDICAL ELECTRODE JELLY?

MAVIDON MEDICAL ELECTRODE JELLY is a medical device that received FDA 510(k) clearance on 2001-08-24. The listed applicant is Mavidon Medical Products. The 510(k) number is K003924.

When did MAVIDON MEDICAL ELECTRODE JELLY receive FDA 510(k) clearance?

MAVIDON MEDICAL ELECTRODE JELLY received FDA 510(k) clearance on 2001-08-24, under 510(k) number K003924.

Who is the listed applicant for MAVIDON MEDICAL ELECTRODE JELLY?

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

What is the FDA product code for MAVIDON MEDICAL ELECTRODE JELLY?

The FDA product code for MAVIDON MEDICAL ELECTRODE JELLY is GYB.

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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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