DISPOSABLE ECG ELECTRODES EASATRACE
K-Number: K850085 · 1985-02-27
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Device Summary
Frequently Asked Questions
What is the DISPOSABLE ECG ELECTRODES EASATRACE?
DISPOSABLE ECG ELECTRODES EASATRACE is a medical device that received FDA 510(k) clearance on 1985-02-27. The listed applicant is Medical Device Marketing. The 510(k) number is K850085.
When did DISPOSABLE ECG ELECTRODES EASATRACE receive FDA 510(k) clearance?
DISPOSABLE ECG ELECTRODES EASATRACE received FDA 510(k) clearance on 1985-02-27, under 510(k) number K850085.
Who is the listed applicant for DISPOSABLE ECG ELECTRODES EASATRACE?
The FDA 510(k) record lists Medical Device Marketing as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DISPOSABLE ECG ELECTRODES EASATRACE?
The FDA product code for DISPOSABLE ECG ELECTRODES EASATRACE 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.
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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