LIFESYNC ADAPTER, MODEL LS-302— 510(k) K071751

Substantially Equivalent

Lifesync Corporation

FDA 510(k) clearance K071751 for LIFESYNC ADAPTER, MODEL LS-302, Substantially Equivalent on 2007-08-27. Applicant: Lifesync Corporation.

Clearance details

Applicant: Lifesync Corporation
Product code: Code DSA
Advisory panel: Cardiovascular
Date received: 2007-06-28
Decision date: 2007-08-27
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Coral Springs, FL, US

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Adverse events under product code DSA

product code DSA

Death: 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.