Medifun Safety Lancet ( MSL1 series)— 510(k) K241750

Substantially Equivalent

Medifun Corporation

FDA 510(k) clearance K241750 for Medifun Safety Lancet ( MSL1 series), Substantially Equivalent on 2024-08-15. Applicant: Medifun Corporation.

Clearance details

Applicant: Medifun Corporation
Product code: Code FMK
Advisory panel: General, Plastic Surgery
Date received: 2024-06-18
Decision date: 2024-08-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Taichung City, TW

Download summary PDF View on FDA.gov ↗

Adverse events under product code FMK

product code FMK

Injury: 133
Malfunction: 1,278
Other: 1
Total: 1,412

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.