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FDA 510(k)

SILICONE DUAL LUMEN RADPICC CATHETERS

K-Number: K030255 · 2003-02-07

Decision Date2003-02-07
Product CodeLJS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SILICONE DUAL LUMEN RADPICC CATHETERS 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 2003-02-07 under 510(k) number K030255. 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 SILICONE DUAL LUMEN RADPICC CATHETERS?

SILICONE DUAL LUMEN RADPICC CATHETERS is a medical device that received FDA 510(k) clearance on 2003-02-07. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K030255.

When did SILICONE DUAL LUMEN RADPICC CATHETERS receive FDA 510(k) clearance?

SILICONE DUAL LUMEN RADPICC CATHETERS received FDA 510(k) clearance on 2003-02-07, under 510(k) number K030255.

Who is the listed applicant for SILICONE DUAL LUMEN RADPICC CATHETERS?

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 SILICONE DUAL LUMEN RADPICC CATHETERS?

The FDA product code for SILICONE DUAL LUMEN RADPICC CATHETERS 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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