3M LITTMANN TELESTETH ONLINE AUSCULATION SYSTEM— 510(k) K120704

Substantially Equivalent

3M Company

FDA 510(k) clearance K120704 for 3M LITTMANN TELESTETH ONLINE AUSCULATION SYSTEM, Substantially Equivalent on 2012-05-03. Applicant: 3M Company.

Clearance details

Applicant: 3M Company
Product code: Code DRG
Advisory panel: Cardiovascular
Date received: 2012-03-08
Decision date: 2012-05-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Paul, MN, US

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Adverse events under product code DRG

product code DRG

Death: 5
Total: 5

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. 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.