VITALLINK3 MOBILE VITAL SIGNS SYSTEM— 510(k) K073094

Substantially Equivalent

Telemedic Systems, Ltd.

FDA 510(k) clearance K073094 for VITALLINK3 MOBILE VITAL SIGNS SYSTEM, Substantially Equivalent on 2008-01-04. Applicant: Telemedic Systems, Ltd..

Clearance details

Applicant: Telemedic Systems, Ltd.
Product code: Code MWI
Advisory panel: Cardiovascular
Date received: 2007-11-01
Decision date: 2008-01-04
Decision: Substantially Equivalent
Clearance type: Special
Location: Taunton, Somerset, GB

Download summary PDF View on FDA.gov ↗

Adverse events under product code MWI

product code MWI

Death: 16
Malfunction: 963
Total: 979

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.