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FDA 510(k)

Boss Crossing Support Catheter

K-Number: K220632 · 2022-06-02

ApplicantMarvao Medical Devices, Ltd.
Decision Date2022-06-02
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Boss Crossing Support Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Marvao Medical Devices, Ltd.. It received FDA 510(k) clearance on 2022-06-02 under 510(k) number K220632. 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 Boss Crossing Support Catheter?

Boss Crossing Support Catheter is a medical device that received FDA 510(k) clearance on 2022-06-02. The listed applicant is Marvao Medical Devices, Ltd.. The 510(k) number is K220632.

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

Boss Crossing Support Catheter received FDA 510(k) clearance on 2022-06-02, under 510(k) number K220632.

Who is the listed applicant for Boss Crossing Support Catheter?

The FDA 510(k) record lists Marvao Medical Devices, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Boss Crossing Support Catheter?

The FDA product code for Boss Crossing Support Catheter is DQY.

Other records listing Marvao Medical Devices, Ltd. as applicant

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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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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