CPR LOCATOR— 510(k) K833737

Substantially Equivalent

Lifepoint,Inc

FDA 510(k) clearance K833737 for CPR LOCATOR, Substantially Equivalent on 1984-08-24. Applicant: Lifepoint,Inc.

Clearance details

Applicant: Lifepoint,Inc
Product code: Code LIX
Advisory panel: Cardiovascular
Date received: 1983-10-25
Decision date: 1984-08-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

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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.