CPRmeter 2 CPR Feedback Device— 510(k) K173886

Substantially Equivalent

Laerdal Medical AS

FDA 510(k) clearance K173886 for CPRmeter 2 CPR Feedback Device, Substantially Equivalent on 2018-03-23. Applicant: Laerdal Medical AS.

Clearance details

Applicant: Laerdal Medical AS
Product code: Code LIX
Advisory panel: Cardiovascular
Date received: 2017-12-21
Decision date: 2018-03-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Stavanger, NO

Download summary PDF View on FDA.gov ↗

Adverse events under product code LIX

product code LIX

Other: 2
Total: 2

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.