LONG TERM CENTRAL VENOUS ACCESS CATH
K-Number: K834299 · 1984-05-01
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Device Summary
Frequently Asked Questions
What is the LONG TERM CENTRAL VENOUS ACCESS CATH?
LONG TERM CENTRAL VENOUS ACCESS CATH is a medical device that received FDA 510(k) clearance on 1984-05-01. The listed applicant is Burron Medical Products, Inc.. The 510(k) number is K834299.
When did LONG TERM CENTRAL VENOUS ACCESS CATH receive FDA 510(k) clearance?
LONG TERM CENTRAL VENOUS ACCESS CATH received FDA 510(k) clearance on 1984-05-01, under 510(k) number K834299.
Who is the listed applicant for LONG TERM CENTRAL VENOUS ACCESS CATH?
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 LONG TERM CENTRAL VENOUS ACCESS CATH?
The FDA product code for LONG TERM CENTRAL VENOUS ACCESS CATH is LJS.
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: LJS)
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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