EM DIAGNOSTIC ECG ELECTRODE
K-Number: K862746 · 1986-08-06
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Device Summary
Frequently Asked Questions
What is the EM DIAGNOSTIC ECG ELECTRODE?
EM DIAGNOSTIC ECG ELECTRODE is a medical device that received FDA 510(k) clearance on 1986-08-06. The listed applicant is Electromed Intl., Ltd.. The 510(k) number is K862746.
When did EM DIAGNOSTIC ECG ELECTRODE receive FDA 510(k) clearance?
EM DIAGNOSTIC ECG ELECTRODE received FDA 510(k) clearance on 1986-08-06, under 510(k) number K862746.
Who is the listed applicant for EM DIAGNOSTIC ECG ELECTRODE?
The FDA 510(k) record lists Electromed Intl., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EM DIAGNOSTIC ECG ELECTRODE?
The FDA product code for EM DIAGNOSTIC ECG ELECTRODE is DRX.
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 Electromed Intl., 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.
Related Devices (Code: DRX)
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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