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FDA 510(k)

KAWASUMI BLOOD TUBING LINE

K-Number: K873516 · 1987-10-05

Decision Date1987-10-05
Product CodeFJK
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

KAWASUMI BLOOD TUBING LINE is the device name listed in this FDA 510(k) record. The listed applicant is Kawasumi Laboratories Co., Ltd.. It received FDA 510(k) clearance on 1987-10-05 under 510(k) number K873516. The device is classified under product code FJK. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 18 devices →

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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