Promisemed Blood Lancet, VeriFine Safety Lancet, VeriFine Mini-Safety Lancet
K-Number: K221368 · 2022-06-09
Device Summary
Frequently Asked Questions
What is the Promisemed Blood Lancet, VeriFine Safety Lancet, VeriFine Mini-Safety Lancet?
Promisemed Blood Lancet, VeriFine Safety Lancet, VeriFine Mini-Safety Lancet is a medical device that received FDA 510(k) clearance on 2022-06-09. The listed applicant is Promisemed Hangzhou Meditech Co., Ltd.. The 510(k) number is K221368.
When did Promisemed Blood Lancet, VeriFine Safety Lancet, VeriFine Mini-Safety Lancet receive FDA 510(k) clearance?
Promisemed Blood Lancet, VeriFine Safety Lancet, VeriFine Mini-Safety Lancet received FDA 510(k) clearance on 2022-06-09, under 510(k) number K221368.
Who is the listed applicant for Promisemed Blood Lancet, VeriFine Safety Lancet, VeriFine Mini-Safety Lancet?
The FDA 510(k) record lists Promisemed Hangzhou Meditech Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Promisemed Blood Lancet, VeriFine Safety Lancet, VeriFine Mini-Safety Lancet?
The FDA product code for Promisemed Blood Lancet, VeriFine Safety Lancet, VeriFine Mini-Safety Lancet is FMK.
Other records listing Promisemed Hangzhou Meditech Co., Ltd. as applicant
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.
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.