Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ACCU-TRODE (DISP. ECG ELECTRODE)

K-Number: K771392 · 1977-08-16

Decision Date1977-08-16
Product CodeDRX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ACCU-TRODE (DISP. ECG ELECTRODE) is the device name listed in this FDA 510(k) record. The listed applicant is Warner/Chilcott. It received FDA 510(k) clearance on 1977-08-16 under 510(k) number K771392. 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 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.

↑