3M RED DOT RESTING EKG ELECTRODE, CATALOG 2360— 510(k) K974445

Substantially Equivalent

3M Healthcare

FDA 510(k) clearance K974445 for 3M RED DOT RESTING EKG ELECTRODE, CATALOG 2360, Substantially Equivalent on 1998-07-26. Applicant: 3M Healthcare. Device class: 2.

Clearance details

Applicant
3M Healthcare
Product code
Code DRX
Device class
Class 2
Regulation
21 CFR 870.2360
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
St. Paul, MN, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code DRX

product code DRX
Death
6
Injury
476
Other
2
Total
484

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.