ARTERIOVENOUS BLOOD TUBING SETS
K-Number: K780681 · 1978-06-14
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Device Summary
Frequently Asked Questions
What is the ARTERIOVENOUS BLOOD TUBING SETS?
ARTERIOVENOUS BLOOD TUBING SETS is a medical device that received FDA 510(k) clearance on 1978-06-14. The listed applicant is Extracorporeal Medical Specialities, Inc.. The 510(k) number is K780681.
When did ARTERIOVENOUS BLOOD TUBING SETS receive FDA 510(k) clearance?
ARTERIOVENOUS BLOOD TUBING SETS received FDA 510(k) clearance on 1978-06-14, under 510(k) number K780681.
Who is the listed applicant for ARTERIOVENOUS BLOOD TUBING SETS?
The FDA 510(k) record lists Extracorporeal Medical Specialities, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ARTERIOVENOUS BLOOD TUBING SETS?
The FDA product code for ARTERIOVENOUS BLOOD TUBING SETS 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 Extracorporeal Medical Specialities, Inc. 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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