LF900
K-Number: K231437 · 2023-07-19
Device Summary
Frequently Asked Questions
What is the LF900?
LF900 is a medical device that received FDA 510(k) clearance on 2023-07-19. The listed applicant is Daesung Maref Co., Ltd.. The 510(k) number is K231437.
When did LF900 receive FDA 510(k) clearance?
LF900 received FDA 510(k) clearance on 2023-07-19, under 510(k) number K231437.
Who is the listed applicant for LF900?
The FDA 510(k) record lists Daesung Maref Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LF900?
The FDA product code for LF900 is IRP.
Other records listing Daesung Maref 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: IRP)
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.