Lancing System, Sterile Lancet for Single Use, Lancing Device— 510(k) K222472
Substantially EquivalentShandong Lianfa Medical Plastic Products Co. , Ltd.
FDA 510(k) clearance K222472 for Lancing System, Sterile Lancet for Single Use, Lancing Device, Substantially Equivalent on 2022-11-30. Applicant: Shandong Lianfa Medical Plastic Products Co. , Ltd.. Device class: 2.
Clearance details
- Applicant
- Shandong Lianfa Medical Plastic Products Co. , Ltd.
- Product code
- Code QRL
- Device class
- Class 2
- Regulation
- 21 CFR 878.4850
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Jinan, CN
Recent devices under product code QRL
view allMore clearances from Shandong Lianfa Medical Plastic Products Co. , Ltd.
view allAdverse events under product code QRL
product code QRL- Other
- 1
- Total
- 1
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Recalls naming K222472
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K222472.
Data sourced from openFDA. This site is unofficial and independent of the FDA.