ARTERIAL VENOUS BLOOD TUBING SET
K-Number: K953823 · 1996-09-23
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Device Summary
Frequently Asked Questions
What is the ARTERIAL VENOUS BLOOD TUBING SET?
ARTERIAL VENOUS BLOOD TUBING SET is a medical device that received FDA 510(k) clearance on 1996-09-23. The listed applicant is Medisystems Corp.. The 510(k) number is K953823.
When did ARTERIAL VENOUS BLOOD TUBING SET receive FDA 510(k) clearance?
ARTERIAL VENOUS BLOOD TUBING SET received FDA 510(k) clearance on 1996-09-23, under 510(k) number K953823.
Who is the listed applicant for ARTERIAL VENOUS BLOOD TUBING SET?
The FDA 510(k) record lists Medisystems Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ARTERIAL VENOUS BLOOD TUBING SET?
The FDA product code for ARTERIAL VENOUS BLOOD TUBING 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 Medisystems 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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