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FDA PMA

Transdermal test for Assessment of Glomerular Filtration Rate

PMA Number: P230019 · 2026-10-02

ApplicantMedibeacon, Inc.
Decision Date2026-10-02
PMA NumberP230019
Product CodeSDK
Device ClassClass 3
Medical SpecialtyU
Advisory CommitteeGU

Device Summary

Transdermal test for Assessment of Glomerular Filtration Rate is the device name listed in this FDA 510(k) record. The listed applicant is Medibeacon, Inc.. It received FDA 510(k) clearance on 2026-10-02. The device is classified under product code SDK. It was reviewed by the GU advisory panel.

Frequently Asked Questions

What is the Transdermal test for Assessment of Glomerular Filtration Rate?

Transdermal test for Assessment of Glomerular Filtration Rate is a medical device that received FDA 510(k) clearance on 2026-10-02. The listed applicant is Medibeacon, Inc..

When did Transdermal test for Assessment of Glomerular Filtration Rate receive FDA 510(k) clearance?

The clearance date for Transdermal test for Assessment of Glomerular Filtration Rate can be found in the official FDA records.

Who is the listed applicant for Transdermal test for Assessment of Glomerular Filtration Rate?

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

What is the FDA product code for Transdermal test for Assessment of Glomerular Filtration Rate?

The FDA product code for Transdermal test for Assessment of Glomerular Filtration Rate is SDK.

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.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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