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FDA 510(k)

Atlas Gold PTA Dilatation Catheter

K-Number: K181323 · 2018-08-03

ApplicantC.R. Bard, Inc.
Decision Date2018-08-03
Product CodeLIT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Atlas Gold PTA Dilatation Catheter is a medical device manufactured by C.R. Bard, Inc.. It received FDA 510(k) clearance on 2018-08-03 under approval number K181323. The device is classified under product code LIT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Atlas Gold PTA Dilatation Catheter?

Atlas Gold PTA Dilatation Catheter is a medical device that received FDA 510(k) clearance on 2018-08-03. It is manufactured by C.R. Bard, Inc.. The 510(k) number is K181323.

When was Atlas Gold PTA Dilatation Catheter approved by the FDA?

Atlas Gold PTA Dilatation Catheter received FDA 510(k) clearance on 2018-08-03, under approval number K181323.

What company makes Atlas Gold PTA Dilatation Catheter?

Atlas Gold PTA Dilatation Catheter is manufactured by C.R. Bard, Inc..

What is the FDA product code for Atlas Gold PTA Dilatation Catheter?

The FDA product code for Atlas Gold PTA Dilatation Catheter is LIT.

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Related Devices (Code: LIT)

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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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