510(k) K223643

Verifine® Ease Lancing Device, Verifine® Lancing Device by Promisemed Hangzhou Meditech Co., Ltd. — Product Code QRL

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 21, 2023
Date Received
December 6, 2022
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Multiple Use Blood Lancet For Single Patient Use Only
Device Class
Class II
Regulation Number
878.4850
Review Panel
SU
Submission Type

A multiple use capable blood lancet intended for use on a single patient that is comprised of a single use blade attached to a solid, reusable base that is used to puncture the skin to obtain a drop of blood for diagnostic purposes.