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FDA 510(k)

MRI POWERPORT IMPLANTED PORT WITH 9.6 FR SILICONE CATHETER

K-Number: K073423 · 2007-12-19

ApplicantC.R. Bard, Inc.
Decision Date2007-12-19
Product CodeLJT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MRI POWERPORT IMPLANTED PORT WITH 9.6 FR SILICONE 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 2007-12-19 under 510(k) number K073423. 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 MRI POWERPORT IMPLANTED PORT WITH 9.6 FR SILICONE CATHETER?

MRI POWERPORT IMPLANTED PORT WITH 9.6 FR SILICONE CATHETER is a medical device that received FDA 510(k) clearance on 2007-12-19. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K073423.

When did MRI POWERPORT IMPLANTED PORT WITH 9.6 FR SILICONE CATHETER receive FDA 510(k) clearance?

MRI POWERPORT IMPLANTED PORT WITH 9.6 FR SILICONE CATHETER received FDA 510(k) clearance on 2007-12-19, under 510(k) number K073423.

Who is the listed applicant for MRI POWERPORT IMPLANTED PORT WITH 9.6 FR SILICONE 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 MRI POWERPORT IMPLANTED PORT WITH 9.6 FR SILICONE CATHETER?

The FDA product code for MRI POWERPORT IMPLANTED PORT WITH 9.6 FR SILICONE CATHETER is 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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