SurgiLance® Safety Lancet
K-Number: K222224 · 2022-09-22
Device Summary
Frequently Asked Questions
What is the SurgiLance® Safety Lancet?
SurgiLance® Safety Lancet is a medical device that received FDA 510(k) clearance on 2022-09-22. The listed applicant is Medipurpose Pte. , Ltd.. The 510(k) number is K222224.
When did SurgiLance® Safety Lancet receive FDA 510(k) clearance?
SurgiLance® Safety Lancet received FDA 510(k) clearance on 2022-09-22, under 510(k) number K222224.
Who is the listed applicant for SurgiLance® Safety Lancet?
The FDA 510(k) record lists Medipurpose Pte. , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SurgiLance® Safety Lancet?
The FDA product code for SurgiLance® Safety Lancet is FMK.
Related Devices (Code: FMK)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.