Verifine Safety Lancets
K-Number: K261045 · 2026-05-01
Decision Date2026-05-01
Product CodeFMK
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
Verifine Safety Lancets is a medical device manufactured by Promisemed Hangzhou Meditech Co., Ltd.. It received FDA 510(k) clearance on 2026-05-01 under approval number K261045. The device is classified under product code FMK. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Verifine Safety Lancets?
Verifine Safety Lancets is a medical device that received FDA 510(k) clearance on 2026-05-01. It is manufactured by Promisemed Hangzhou Meditech Co., Ltd.. The 510(k) number is K261045.
When was Verifine Safety Lancets approved by the FDA?
Verifine Safety Lancets received FDA 510(k) clearance on 2026-05-01, under approval number K261045.
What company makes Verifine Safety Lancets?
Verifine Safety Lancets is manufactured by Promisemed Hangzhou Meditech Co., Ltd..
What is the FDA product code for Verifine Safety Lancets?
The FDA product code for Verifine Safety Lancets is FMK.
Other Devices by Promisemed Hangzhou Meditech Co., Ltd.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.