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FDA 510(k)

Recon Support Catheter

K-Number: K203275 · 2021-03-01

ApplicantC.R. Bard, Inc.
Decision Date2021-03-01
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Recon Support 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 2021-03-01 under 510(k) number K203275. 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 Recon Support Catheter?

Recon Support Catheter is a medical device that received FDA 510(k) clearance on 2021-03-01. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K203275.

When did Recon Support Catheter receive FDA 510(k) clearance?

Recon Support Catheter received FDA 510(k) clearance on 2021-03-01, under 510(k) number K203275.

Who is the listed applicant for Recon Support 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 Recon Support Catheter?

The FDA product code for Recon Support Catheter is DQY.

Related Clinical Trials

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Other records listing C.R. Bard, Inc. as applicant

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Related Devices (Code: DQY)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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