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FDA 510(k)

POWERPORT CLEARVUE SLIM IMPLANTABLE PORT

K-Number: K122899 · 2012-11-15

Decision Date2012-11-15
Product CodeLJT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

POWERPORT CLEARVUE SLIM IMPLANTABLE PORT 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 2012-11-15 under 510(k) number K122899. The device is classified under product code LJT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POWERPORT CLEARVUE SLIM IMPLANTABLE PORT?

POWERPORT CLEARVUE SLIM IMPLANTABLE PORT is a medical device that received FDA 510(k) clearance on 2012-11-15. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K122899.

When did POWERPORT CLEARVUE SLIM IMPLANTABLE PORT receive FDA 510(k) clearance?

POWERPORT CLEARVUE SLIM IMPLANTABLE PORT received FDA 510(k) clearance on 2012-11-15, under 510(k) number K122899.

Who is the listed applicant for POWERPORT CLEARVUE SLIM IMPLANTABLE PORT?

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 POWERPORT CLEARVUE SLIM IMPLANTABLE PORT?

The FDA product code for POWERPORT CLEARVUE SLIM IMPLANTABLE PORT is LJT.

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: LJT)

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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