DOCXS B SERIES ELECTRODES
K-Number: K020903 · 2002-09-26
Advertisement
Device Summary
Frequently Asked Questions
What is the DOCXS B SERIES ELECTRODES?
DOCXS B SERIES ELECTRODES is a medical device that received FDA 510(k) clearance on 2002-09-26. The listed applicant is Docxs, LLC. The 510(k) number is K020903.
When did DOCXS B SERIES ELECTRODES receive FDA 510(k) clearance?
DOCXS B SERIES ELECTRODES received FDA 510(k) clearance on 2002-09-26, under 510(k) number K020903.
Who is the listed applicant for DOCXS B SERIES ELECTRODES?
The FDA 510(k) record lists Docxs, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DOCXS B SERIES ELECTRODES?
The FDA product code for DOCXS B SERIES ELECTRODES is GXY.
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.
Related Devices (Code: GXY)
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.
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.
Advertisement