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FDA 510(k)

6 FR POLY PER-Q-CATH TRIPLE LUMEN PICC

K-Number: K043502 · 2005-01-14

Decision Date2005-01-14
Product CodeLJS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

6 FR POLY PER-Q-CATH TRIPLE LUMEN PICC is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 2005-01-14 under 510(k) number K043502. The device is classified under product code LJS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 616 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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