TRUSCOPE SERIES PATIENT MONITOR— 510(k) K131763

Substantially Equivalent

Guangdong Biolight Meditech Co., Ltd.

FDA 510(k) clearance K131763 for TRUSCOPE SERIES PATIENT MONITOR, Substantially Equivalent on 2013-07-15. Applicant: Guangdong Biolight Meditech Co., Ltd..

Clearance details

Applicant: Guangdong Biolight Meditech Co., Ltd.
Product code: Code MHX
Advisory panel: Cardiovascular
Date received: 2013-06-17
Decision date: 2013-07-15
Decision: Substantially Equivalent
Clearance type: Special
Location: Shanghai, CN

Download summary PDF View on FDA.gov ↗

Adverse events under product code MHX

product code MHX

Death: 580
Injury: 2,441
Malfunction: 12,655
Other: 3
Total: 15,679

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.