MULTI-DAY ELECTRODES
K-Number: K862011 · 1986-07-03
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Device Summary
Frequently Asked Questions
What is the MULTI-DAY ELECTRODES?
MULTI-DAY ELECTRODES is a medical device that received FDA 510(k) clearance on 1986-07-03. The listed applicant is Medical Electronic Assn.. The 510(k) number is K862011.
When did MULTI-DAY ELECTRODES receive FDA 510(k) clearance?
MULTI-DAY ELECTRODES received FDA 510(k) clearance on 1986-07-03, under 510(k) number K862011.
Who is the listed applicant for MULTI-DAY ELECTRODES?
The FDA 510(k) record lists Medical Electronic Assn. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MULTI-DAY ELECTRODES?
The FDA product code for MULTI-DAY 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.
Other records listing Medical Electronic Assn. 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.
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.
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