510(k) K223480
K223480 is an FDA 510(k) premarket notification submitted by Medipoint Holdings, LLC for the device "Medipoint Blood Lancets". The FDA issued a decision of Substantially Equivalent on January 13, 2023. The device falls under product code QRK (Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention Feature), a Class II device regulated under 21 CFR 878.4850.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 13, 2023
- Date Received
- November 18, 2022
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention Feature
- Device Class
- Class II
- Regulation Number
- 878.4850
- Review Panel
- SU
- Submission Type
A disposable blood lancet intended for a single use that is comprised of a single use blade attached to a solid, nonreusable base that is used to puncture the skin to obtain a drop of blood for diagnostic purposes.