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FDA 510(k)

MD MONITORING/DIAGNOSTIC ELECTRODE

K-Number: K870873 · 1987-04-10

ApplicantLectec Corp.
Decision Date1987-04-10
Product CodeDRX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MD MONITORING/DIAGNOSTIC ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Lectec Corp.. It received FDA 510(k) clearance on 1987-04-10 under 510(k) number K870873. The device is classified under product code DRX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 27 devices →

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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