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FDA 510(k)

X-FORCE N30 NEPHROSTOMY BALLOON DILATION CATHETER

K-Number: K063632 · 2007-01-05

ApplicantC.R. Bard, Inc.
Decision Date2007-01-05
Product CodeLJE
DecisionSubstantially Equivalent

Device Summary

X-FORCE N30 NEPHROSTOMY BALLOON DILATION 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 2007-01-05 under 510(k) number K063632. The device is classified under product code LJE. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the X-FORCE N30 NEPHROSTOMY BALLOON DILATION CATHETER?

X-FORCE N30 NEPHROSTOMY BALLOON DILATION CATHETER is a medical device that received FDA 510(k) clearance on 2007-01-05. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K063632.

When did X-FORCE N30 NEPHROSTOMY BALLOON DILATION CATHETER receive FDA 510(k) clearance?

X-FORCE N30 NEPHROSTOMY BALLOON DILATION CATHETER received FDA 510(k) clearance on 2007-01-05, under 510(k) number K063632.

Who is the listed applicant for X-FORCE N30 NEPHROSTOMY BALLOON DILATION 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 X-FORCE N30 NEPHROSTOMY BALLOON DILATION CATHETER?

The FDA product code for X-FORCE N30 NEPHROSTOMY BALLOON DILATION CATHETER is LJE.

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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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