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FDA 510(k)

4 FR SINGLE LUMEN (SL) POWERPICC CATHETER

K-Number: K070996 · 2007-05-08

ApplicantC.R. Bard, Inc.
Decision Date2007-05-08
Product CodeLJS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

4 FR SINGLE LUMEN (SL) POWERPICC 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 2007-05-08 under 510(k) number K070996. 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 4 FR SINGLE LUMEN (SL) POWERPICC CATHETER?

4 FR SINGLE LUMEN (SL) POWERPICC CATHETER is a medical device that received FDA 510(k) clearance on 2007-05-08. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K070996.

When did 4 FR SINGLE LUMEN (SL) POWERPICC CATHETER receive FDA 510(k) clearance?

4 FR SINGLE LUMEN (SL) POWERPICC CATHETER received FDA 510(k) clearance on 2007-05-08, under 510(k) number K070996.

Who is the listed applicant for 4 FR SINGLE LUMEN (SL) POWERPICC 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 4 FR SINGLE LUMEN (SL) POWERPICC CATHETER?

The FDA product code for 4 FR SINGLE LUMEN (SL) POWERPICC CATHETER is LJS.

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Related Devices (Code: LJS)

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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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