ACCU-TRODE (DISP. ECG ELECTRODE)
K-Number: K771392 · 1977-08-16
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Device Summary
Frequently Asked Questions
What is the ACCU-TRODE (DISP. ECG ELECTRODE)?
ACCU-TRODE (DISP. ECG ELECTRODE) is a medical device that received FDA 510(k) clearance on 1977-08-16. The listed applicant is Warner/Chilcott. The 510(k) number is K771392.
When did ACCU-TRODE (DISP. ECG ELECTRODE) receive FDA 510(k) clearance?
ACCU-TRODE (DISP. ECG ELECTRODE) received FDA 510(k) clearance on 1977-08-16, under 510(k) number K771392.
Who is the listed applicant for ACCU-TRODE (DISP. ECG ELECTRODE)?
The FDA 510(k) record lists Warner/Chilcott as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACCU-TRODE (DISP. ECG ELECTRODE)?
The FDA product code for ACCU-TRODE (DISP. 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.
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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