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FDA 510(k)

Tigertriever and Tigertriever 17 Revascularization Devce

K-Number: K203592 · 2021-03-23

Decision Date2021-03-23
Product CodeNRY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Tigertriever and Tigertriever 17 Revascularization Devce 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 2021-03-23 under 510(k) number K203592. 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 and Tigertriever 17 Revascularization Devce?

Tigertriever and Tigertriever 17 Revascularization Devce is a medical device that received FDA 510(k) clearance on 2021-03-23. The listed applicant is Rapid Medical , Ltd.. The 510(k) number is K203592.

When did Tigertriever and Tigertriever 17 Revascularization Devce receive FDA 510(k) clearance?

Tigertriever and Tigertriever 17 Revascularization Devce received FDA 510(k) clearance on 2021-03-23, under 510(k) number K203592.

Who is the listed applicant for Tigertriever and Tigertriever 17 Revascularization Devce?

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 and Tigertriever 17 Revascularization Devce?

The FDA product code for Tigertriever and Tigertriever 17 Revascularization Devce 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.