MOOR LASER BLOOD FLOW MONITOR MBF3— 510(k) K905232

Substantially Equivalent

Moor Instruments, Ltd.

FDA 510(k) clearance K905232 for MOOR LASER BLOOD FLOW MONITOR MBF3, Substantially Equivalent on 1991-01-11. Applicant: Moor Instruments, Ltd..

Clearance details

Applicant: Moor Instruments, Ltd.
Product code: Code GEX
Advisory panel: General, Plastic Surgery
Date received: 1990-11-20
Decision date: 1991-01-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Axminster, Devon, GB

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Adverse events under product code GEX

product code GEX

Death: 33
Injury: 3,045
Malfunction: 12,903
Other: 25
Total: 16,006

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.