3M Red Dot 2237 Sticky Gel Monitoring ECG Electrode
FDA 510(k) K934333 · 3M Medical Products Group
510(k) numberK934333
Submission
- Device name
- 3M Red Dot 2237 Sticky Gel Monitoring ECG Electrode
- Applicant
- 3M Medical Products Group
St Paul, MN, US - Received
- September 7, 1993
- Decision date
- July 7, 1994
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
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 2237 Sticky Gel Monitoring ECG Electrode cleared by the FDA?
3M Red Dot 2237 Sticky Gel Monitoring ECG Electrode (K934333) received a 510(k) decision of Substantially Equivalent on July 7, 1994, 303 days after the submission was received.
What is the product code of K934333?
The FDA product code is DRX – Electrode, Electrocardiograph, a Class II (moderate risk) device regulated under 21 CFR 870.2360.