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FDA 510(k)

NORTH COAST BUFFERED IONTOPHORESIS ELECTRODE

K-Number: K052019 · 2005-11-04

ApplicantNorth Coast Medical, Inc.
Decision Date2005-11-04
Product CodeEGJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

NORTH COAST BUFFERED IONTOPHORESIS ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is North Coast Medical, Inc.. It received FDA 510(k) clearance on 2005-11-04 under 510(k) number K052019. The device is classified under product code EGJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NORTH COAST BUFFERED IONTOPHORESIS ELECTRODE?

NORTH COAST BUFFERED IONTOPHORESIS ELECTRODE is a medical device that received FDA 510(k) clearance on 2005-11-04. The listed applicant is North Coast Medical, Inc.. The 510(k) number is K052019.

When did NORTH COAST BUFFERED IONTOPHORESIS ELECTRODE receive FDA 510(k) clearance?

NORTH COAST BUFFERED IONTOPHORESIS ELECTRODE received FDA 510(k) clearance on 2005-11-04, under 510(k) number K052019.

Who is the listed applicant for NORTH COAST BUFFERED IONTOPHORESIS ELECTRODE?

The FDA 510(k) record lists North Coast Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NORTH COAST BUFFERED IONTOPHORESIS ELECTRODE?

The FDA product code for NORTH COAST BUFFERED IONTOPHORESIS ELECTRODE is EGJ.

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Related Devices (Code: EGJ)

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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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