Spacelabs Lifescreen PRO Analyzer— 510(k) K201921

Substantially Equivalent

Spacelabs Healthcare, Ltd.

FDA 510(k) clearance K201921 for Spacelabs Lifescreen PRO Analyzer, Substantially Equivalent on 2021-03-26. Applicant: Spacelabs Healthcare, Ltd..

Clearance details

Applicant: Spacelabs Healthcare, Ltd.
Product code: Code DQK
Advisory panel: Cardiovascular
Date received: 2020-07-10
Decision date: 2021-03-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hertford, GB

Download summary PDF View on FDA.gov ↗

Adverse events under product code DQK

product code DQK

Death: 10
Injury: 225
Malfunction: 2,123
Other: 2
Total: 2,360

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.