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FDA 510(k)

DORADO PTA BALLOON DILATATION CATHETER

K-Number: K072283 · 2007-09-19

ApplicantBard Peripheral Vascular, Inc.
Decision Date2007-09-19
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DORADO 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 2007-09-19 under 510(k) number K072283. 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 DORADO PTA BALLOON DILATATION CATHETER?

DORADO PTA BALLOON DILATATION CATHETER is a medical device that received FDA 510(k) clearance on 2007-09-19. The listed applicant is Bard Peripheral Vascular, Inc.. The 510(k) number is K072283.

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

DORADO PTA BALLOON DILATATION CATHETER received FDA 510(k) clearance on 2007-09-19, under 510(k) number K072283.

Who is the listed applicant for DORADO 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 DORADO PTA BALLOON DILATATION CATHETER?

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

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Related Devices (Code: 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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