MD MONITORING/DIAGNOSTIC ELECTRODE
K-Number: K870873 · 1987-04-10
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Device Summary
Frequently Asked Questions
What is the MD MONITORING/DIAGNOSTIC ELECTRODE?
MD MONITORING/DIAGNOSTIC ELECTRODE is a medical device that received FDA 510(k) clearance on 1987-04-10. The listed applicant is Lectec Corp.. The 510(k) number is K870873.
When did MD MONITORING/DIAGNOSTIC ELECTRODE receive FDA 510(k) clearance?
MD MONITORING/DIAGNOSTIC ELECTRODE received FDA 510(k) clearance on 1987-04-10, under 510(k) number K870873.
Who is the listed applicant for MD MONITORING/DIAGNOSTIC ELECTRODE?
The FDA 510(k) record lists Lectec Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MD MONITORING/DIAGNOSTIC ELECTRODE?
The FDA product code for MD MONITORING/DIAGNOSTIC 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 Lectec Corp. 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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