MedtFine Safety Lancet
K-Number: K241848 · 2024-08-20
Device Summary
Frequently Asked Questions
What is the MedtFine Safety Lancet?
MedtFine Safety Lancet is a medical device that received FDA 510(k) clearance on 2024-08-20. The listed applicant is Ningbo Caremed Medical Products Co., Ltd.. The 510(k) number is K241848.
When did MedtFine Safety Lancet receive FDA 510(k) clearance?
MedtFine Safety Lancet received FDA 510(k) clearance on 2024-08-20, under 510(k) number K241848.
Who is the listed applicant for MedtFine Safety Lancet?
The FDA 510(k) record lists Ningbo Caremed Medical Products Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MedtFine Safety Lancet?
The FDA product code for MedtFine Safety Lancet is FMK.
Other records listing Ningbo Caremed Medical Products 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.