510(k) clearance
Lancing device
- 510(k) number
- K262135
- Applicant
- Tianjin Huahong Technology Co., Ltd.
- Decision date
- Aug 18, 2026
- Date received
- Jun 25, 2026
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Product code
- QRL
- Device type
- Multiple Use Blood Lancet For Single Patient Use Only
- Device class
- Class II
- Regulation
- 21 CFR 878.4850
- Advisory committee
- General, Plastic Surgery
- Statement or summary
- Summary
- Third party
- N
- Location
- Tianjin, CN