REXEED SERIES DIALYZERS
K-Number: K051187 · 2005-06-08
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Device Summary
Frequently Asked Questions
What is the REXEED SERIES DIALYZERS?
REXEED SERIES DIALYZERS is a medical device that received FDA 510(k) clearance on 2005-06-08. The listed applicant is Asahi Kasei Medical Co., Ltd.. The 510(k) number is K051187.
When did REXEED SERIES DIALYZERS receive FDA 510(k) clearance?
REXEED SERIES DIALYZERS received FDA 510(k) clearance on 2005-06-08, under 510(k) number K051187.
Who is the listed applicant for REXEED SERIES DIALYZERS?
The FDA 510(k) record lists Asahi Kasei Medical Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for REXEED SERIES DIALYZERS?
The FDA product code for REXEED SERIES DIALYZERS is KDI.
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 Asahi Kasei Medical 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: KDI)
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.
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