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FDA 510(k)

BARD ATLAS PTA BALLOON DILATATION CATHETER

K-Number: K052236 · 2005-08-23

ApplicantBard Peripheral Vascular, Inc.
Decision Date2005-08-23
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BARD ATLAS PTA BALLOON DILATATION CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Bard Peripheral Vascular, Inc.. It received FDA 510(k) clearance on 2005-08-23 under 510(k) number K052236. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARD ATLAS PTA BALLOON DILATATION CATHETER?

BARD ATLAS PTA BALLOON DILATATION CATHETER is a medical device that received FDA 510(k) clearance on 2005-08-23. The listed applicant is Bard Peripheral Vascular, Inc.. The 510(k) number is K052236.

When did BARD ATLAS PTA BALLOON DILATATION CATHETER receive FDA 510(k) clearance?

BARD ATLAS PTA BALLOON DILATATION CATHETER received FDA 510(k) clearance on 2005-08-23, under 510(k) number K052236.

Who is the listed applicant for BARD ATLAS PTA BALLOON DILATATION CATHETER?

The FDA 510(k) record lists Bard Peripheral Vascular, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BARD ATLAS PTA BALLOON DILATATION CATHETER?

The FDA product code for BARD ATLAS PTA BALLOON DILATATION CATHETER is DQY.

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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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