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FDA 510(k)

Tigertriever 25 Revascularization Device

K-Number: K253062 · 2026-03-12

Decision Date2026-03-12
Product CodeNRY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Tigertriever 25 Revascularization Device is the device name listed in this FDA 510(k) record. The listed applicant is Rapid Medical Ltd.. It received FDA 510(k) clearance on 2026-03-12 under 510(k) number K253062. The device is classified under product code NRY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Tigertriever 25 Revascularization Device?

Tigertriever 25 Revascularization Device is a medical device that received FDA 510(k) clearance on 2026-03-12. The listed applicant is Rapid Medical Ltd.. The 510(k) number is K253062.

When did Tigertriever 25 Revascularization Device receive FDA 510(k) clearance?

Tigertriever 25 Revascularization Device received FDA 510(k) clearance on 2026-03-12, under 510(k) number K253062.

Who is the listed applicant for Tigertriever 25 Revascularization Device?

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

What is the FDA product code for Tigertriever 25 Revascularization Device?

The FDA product code for Tigertriever 25 Revascularization Device is NRY.

Related Clinical Trials

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.

Other records listing Rapid Medical 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: NRY)

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.

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.