Safety Lancet (XIII, XVII, XXI, XXII, XXIII, XXIV, XXV, XXVI)— 510(k) K220370

Substantially Equivalent

Tianjin Huahong Technology Co., Ltd.

FDA 510(k) clearance K220370 for Safety Lancet (XIII, XVII, XXI, XXII, XXIII, XXIV, XXV, XXVI), Substantially Equivalent on 2022-05-19. Applicant: Tianjin Huahong Technology Co., Ltd..

Clearance details

Applicant: Tianjin Huahong Technology Co., Ltd.
Product code: Code FMK
Advisory panel: General, Plastic Surgery
Date received: 2022-02-09
Decision date: 2022-05-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tianjin, CN

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.