6 FR POLY PER-Q-CATH TRIPLE LUMEN PICC
K-Number: K043502 · 2005-01-14
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Device Summary
Frequently Asked Questions
What is the 6 FR POLY PER-Q-CATH TRIPLE LUMEN PICC?
6 FR POLY PER-Q-CATH TRIPLE LUMEN PICC is a medical device that received FDA 510(k) clearance on 2005-01-14. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K043502.
When did 6 FR POLY PER-Q-CATH TRIPLE LUMEN PICC receive FDA 510(k) clearance?
6 FR POLY PER-Q-CATH TRIPLE LUMEN PICC received FDA 510(k) clearance on 2005-01-14, under 510(k) number K043502.
Who is the listed applicant for 6 FR POLY PER-Q-CATH TRIPLE LUMEN PICC?
The FDA 510(k) record lists C.R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 6 FR POLY PER-Q-CATH TRIPLE LUMEN PICC?
The FDA product code for 6 FR POLY PER-Q-CATH TRIPLE LUMEN PICC 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 C.R. Bard, 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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