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FDA 510(k)

POWERPORT POLYMETRIC PORT WITH 8 FR S/L CHRONOFLEX CATHETER

K-Number: K063377 · 2007-01-25

ApplicantC.R. Bard, Inc.
Decision Date2007-01-25
Product CodeLJT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

POWERPORT POLYMETRIC PORT WITH 8 FR S/L CHRONOFLEX CATHETER 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 2007-01-25 under 510(k) number K063377. 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 POLYMETRIC PORT WITH 8 FR S/L CHRONOFLEX CATHETER?

POWERPORT POLYMETRIC PORT WITH 8 FR S/L CHRONOFLEX CATHETER is a medical device that received FDA 510(k) clearance on 2007-01-25. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K063377.

When did POWERPORT POLYMETRIC PORT WITH 8 FR S/L CHRONOFLEX CATHETER receive FDA 510(k) clearance?

POWERPORT POLYMETRIC PORT WITH 8 FR S/L CHRONOFLEX CATHETER received FDA 510(k) clearance on 2007-01-25, under 510(k) number K063377.

Who is the listed applicant for POWERPORT POLYMETRIC PORT WITH 8 FR S/L CHRONOFLEX CATHETER?

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 POLYMETRIC PORT WITH 8 FR S/L CHRONOFLEX CATHETER?

The FDA product code for POWERPORT POLYMETRIC PORT WITH 8 FR S/L CHRONOFLEX CATHETER is LJT.

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Related Devices (Code: LJT)

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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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