MULTI-LUMEN CENTRAL VENOUS CATH. KIT
K-Number: K834473 · 1984-04-30
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Device Summary
Frequently Asked Questions
What is the MULTI-LUMEN CENTRAL VENOUS CATH. KIT?
MULTI-LUMEN CENTRAL VENOUS CATH. KIT is a medical device that received FDA 510(k) clearance on 1984-04-30. The listed applicant is Burron Medical Products, Inc.. The 510(k) number is K834473.
When did MULTI-LUMEN CENTRAL VENOUS CATH. KIT receive FDA 510(k) clearance?
MULTI-LUMEN CENTRAL VENOUS CATH. KIT received FDA 510(k) clearance on 1984-04-30, under 510(k) number K834473.
Who is the listed applicant for MULTI-LUMEN CENTRAL VENOUS CATH. 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 MULTI-LUMEN CENTRAL VENOUS CATH. KIT?
The FDA product code for MULTI-LUMEN CENTRAL VENOUS CATH. KIT 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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