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FDA 510(k)

3M RED DOT RESTING EKG ELECTRODE, CATALOG 2360

K-Number: K974445 · 1998-07-26

Applicant3M Healthcare
Decision Date1998-07-26
Product CodeDRX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

3M RED DOT RESTING EKG ELECTRODE, CATALOG 2360 is the device name listed in this FDA 510(k) record. The listed applicant is 3M Healthcare. It received FDA 510(k) clearance on 1998-07-26 under 510(k) number K974445. 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 3M RED DOT RESTING EKG ELECTRODE, CATALOG 2360?

3M RED DOT RESTING EKG ELECTRODE, CATALOG 2360 is a medical device that received FDA 510(k) clearance on 1998-07-26. The listed applicant is 3M Healthcare. The 510(k) number is K974445.

When did 3M RED DOT RESTING EKG ELECTRODE, CATALOG 2360 receive FDA 510(k) clearance?

3M RED DOT RESTING EKG ELECTRODE, CATALOG 2360 received FDA 510(k) clearance on 1998-07-26, under 510(k) number K974445.

Who is the listed applicant for 3M RED DOT RESTING EKG ELECTRODE, CATALOG 2360?

The FDA 510(k) record lists 3M Healthcare as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 3M RED DOT RESTING EKG ELECTRODE, CATALOG 2360?

The FDA product code for 3M RED DOT RESTING EKG ELECTRODE, CATALOG 2360 is DRX.

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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.

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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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