INFUSION CATHETER EXTENSION SET
K-Number: K023224 · 2002-10-25
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Device Summary
Frequently Asked Questions
What is the INFUSION CATHETER EXTENSION SET?
INFUSION CATHETER EXTENSION SET is a medical device that received FDA 510(k) clearance on 2002-10-25. The listed applicant is Chf Solutions, Inc.. The 510(k) number is K023224.
When did INFUSION CATHETER EXTENSION SET receive FDA 510(k) clearance?
INFUSION CATHETER EXTENSION SET received FDA 510(k) clearance on 2002-10-25, under 510(k) number K023224.
Who is the listed applicant for INFUSION CATHETER EXTENSION SET?
The FDA 510(k) record lists Chf Solutions, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INFUSION CATHETER EXTENSION SET?
The FDA product code for INFUSION CATHETER EXTENSION SET 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 Chf Solutions, Inc. 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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