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FDA 510(k)

MEDTRADE PRODICT'S SOOTHING GEL PATCH

K-Number: K030901 · 2004-11-26

Decision Date2004-11-26
Product CodeNTC
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MEDTRADE PRODICT'S SOOTHING GEL PATCH is the device name listed in this FDA 510(k) record. The listed applicant is Medtrade Products , Ltd.. It received FDA 510(k) clearance on 2004-11-26 under 510(k) number K030901. The device is classified under product code NTC. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDTRADE PRODICT'S SOOTHING GEL PATCH?

MEDTRADE PRODICT'S SOOTHING GEL PATCH is a medical device that received FDA 510(k) clearance on 2004-11-26. The listed applicant is Medtrade Products , Ltd.. The 510(k) number is K030901.

When did MEDTRADE PRODICT'S SOOTHING GEL PATCH receive FDA 510(k) clearance?

MEDTRADE PRODICT'S SOOTHING GEL PATCH received FDA 510(k) clearance on 2004-11-26, under 510(k) number K030901.

Who is the listed applicant for MEDTRADE PRODICT'S SOOTHING GEL PATCH?

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

What is the FDA product code for MEDTRADE PRODICT'S SOOTHING GEL PATCH?

The FDA product code for MEDTRADE PRODICT'S SOOTHING GEL PATCH is NTC.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Medtrade Products , Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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