KAWASUMI BLOOD TUBING LINE
K-Number: K873516 · 1987-10-05
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Device Summary
Frequently Asked Questions
What is the KAWASUMI BLOOD TUBING LINE?
KAWASUMI BLOOD TUBING LINE is a medical device that received FDA 510(k) clearance on 1987-10-05. The listed applicant is Kawasumi Laboratories Co., Ltd.. The 510(k) number is K873516.
When did KAWASUMI BLOOD TUBING LINE receive FDA 510(k) clearance?
KAWASUMI BLOOD TUBING LINE received FDA 510(k) clearance on 1987-10-05, under 510(k) number K873516.
Who is the listed applicant for KAWASUMI BLOOD TUBING LINE?
The FDA 510(k) record lists Kawasumi Laboratories Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KAWASUMI BLOOD TUBING LINE?
The FDA product code for KAWASUMI BLOOD TUBING LINE is FJK.
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 Kawasumi Laboratories 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: FJK)
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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