HEMODIALYSIS BLOOD LINES
K-Number: K900306 · 1990-04-20
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Device Summary
Frequently Asked Questions
What is the HEMODIALYSIS BLOOD LINES?
HEMODIALYSIS BLOOD LINES is a medical device that received FDA 510(k) clearance on 1990-04-20. The listed applicant is Gainor Medical Europe, Ltd.. The 510(k) number is K900306.
When did HEMODIALYSIS BLOOD LINES receive FDA 510(k) clearance?
HEMODIALYSIS BLOOD LINES received FDA 510(k) clearance on 1990-04-20, under 510(k) number K900306.
Who is the listed applicant for HEMODIALYSIS BLOOD LINES?
The FDA 510(k) record lists Gainor Medical Europe, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HEMODIALYSIS BLOOD LINES?
The FDA product code for HEMODIALYSIS BLOOD LINES is KOC.
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 Gainor Medical Europe, 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: KOC)
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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