SYSMEX UF-50
K-Number: K012372 · 2001-09-28
Advertisement
Device Summary
Frequently Asked Questions
What is the SYSMEX UF-50?
SYSMEX UF-50 is a medical device that received FDA 510(k) clearance on 2001-09-28. The listed applicant is Sysmex Corp.. The 510(k) number is K012372.
When did SYSMEX UF-50 receive FDA 510(k) clearance?
SYSMEX UF-50 received FDA 510(k) clearance on 2001-09-28, under 510(k) number K012372.
Who is the listed applicant for SYSMEX UF-50?
The FDA 510(k) record lists Sysmex Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SYSMEX UF-50?
The FDA product code for SYSMEX UF-50 is LKM.
Related Clinical Trials
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.
Other records listing Sysmex Corp. 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: LKM)
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.
Advertisement