3M Red Dot 2560 & 2570 Monitoring Electrodes

FDA 510(k) K970796 · 3M Healthcare

Substantially Equivalent

510(k) numberK970796

Submission

Device name
3M Red Dot 2560 & 2570 Monitoring Electrodes
Applicant
3M Healthcare
St. Paul, MN, US
Received
March 4, 1997
Decision date
April 9, 1997
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DRX – Electrode, Electrocardiograph
Device class
Class II (moderate risk)
Regulation
21 CFR 870.2360
Specialty
Cardiovascular

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Questions and answers

When was 3M Red Dot 2560 & 2570 Monitoring Electrodes cleared by the FDA?

3M Red Dot 2560 & 2570 Monitoring Electrodes (K970796) received a 510(k) decision of Substantially Equivalent on April 9, 1997, 36 days after the submission was received.

What is the product code of K970796?

The FDA product code is DRX – Electrode, Electrocardiograph, a Class II (moderate risk) device regulated under 21 CFR 870.2360.