SILICONE DUAL LUMEN RADPICC CATHETERS
K-Number: K030255 · 2003-02-07
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Device Summary
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.
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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