CAVAFIX, CENTRAL VENOUS CATHETER KIT
K-Number: K861479 · 1986-07-01
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Device Summary
Frequently Asked Questions
What is the CAVAFIX, CENTRAL VENOUS CATHETER KIT?
CAVAFIX, CENTRAL VENOUS CATHETER KIT is a medical device that received FDA 510(k) clearance on 1986-07-01. The listed applicant is Burron Medical Products, Inc.. The 510(k) number is K861479.
When did CAVAFIX, CENTRAL VENOUS CATHETER KIT receive FDA 510(k) clearance?
CAVAFIX, CENTRAL VENOUS CATHETER KIT received FDA 510(k) clearance on 1986-07-01, under 510(k) number K861479.
Who is the listed applicant for CAVAFIX, CENTRAL VENOUS CATHETER KIT?
The FDA 510(k) record lists Burron Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CAVAFIX, CENTRAL VENOUS CATHETER KIT?
The FDA product code for CAVAFIX, CENTRAL VENOUS CATHETER KIT is FOZ.
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 Burron Medical Products, 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: FOZ)
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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