TERUMO(R) ARTERIAL AND VENOUS BLOOD LINE SET
K-Number: K910558 · 1991-08-07
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Device Summary
Frequently Asked Questions
What is the TERUMO(R) ARTERIAL AND VENOUS BLOOD LINE SET?
TERUMO(R) ARTERIAL AND VENOUS BLOOD LINE SET is a medical device that received FDA 510(k) clearance on 1991-08-07. The listed applicant is Terumo Medical Corp.. The 510(k) number is K910558.
When did TERUMO(R) ARTERIAL AND VENOUS BLOOD LINE SET receive FDA 510(k) clearance?
TERUMO(R) ARTERIAL AND VENOUS BLOOD LINE SET received FDA 510(k) clearance on 1991-08-07, under 510(k) number K910558.
Who is the listed applicant for TERUMO(R) ARTERIAL AND VENOUS BLOOD LINE SET?
The FDA 510(k) record lists Terumo Medical Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TERUMO(R) ARTERIAL AND VENOUS BLOOD LINE SET?
The FDA product code for TERUMO(R) ARTERIAL AND VENOUS BLOOD LINE SET 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 Terumo Medical Corp. 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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