FDA 510(k)

PATH BGC

K-Number: K242392 · 2025-05-09

Decision Date2025-05-09

Product CodeQJP

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

PATH BGC is the device name listed in this FDA 510(k) record. The listed applicant is Crossroads Neurovascular, Inc.. It received FDA 510(k) clearance on 2025-05-09 under 510(k) 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. The listed applicant is Crossroads Neurovascular, Inc.. The 510(k) number is K242392.

When did PATH BGC receive FDA 510(k) clearance?

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

Who is the listed applicant for PATH BGC?

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

What is the FDA product code for PATH BGC?

The FDA product code for PATH BGC is QJP.

Other records listing Crossroads Neurovascular, Inc. 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.

K260938PATH BGC

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.