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FDA 510(k)

PATH BGC

K-Number: K242392 · 2025-05-09

ApplicantCrossroads Neurovascular, Inc.
Decision Date2025-05-09
Product CodeQJP
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PATH BGC is a medical device manufactured by Crossroads Neurovascular, Inc.. It received FDA 510(k) clearance on 2025-05-09 under approval number K242392. The device is classified under product code QJP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PATH BGC?

PATH BGC is a medical device that received FDA 510(k) clearance on 2025-05-09. It is manufactured by Crossroads Neurovascular, Inc.. The 510(k) number is K242392.

When was PATH BGC approved by the FDA?

PATH BGC received FDA 510(k) clearance on 2025-05-09, under approval number K242392.

What company makes PATH BGC?

PATH BGC is manufactured by Crossroads Neurovascular, Inc..

What is the FDA product code for PATH BGC?

The FDA product code for PATH BGC is QJP.

Other Devices by Crossroads Neurovascular, Inc.

K260938PATH BGC

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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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