Triever Catheters
K-Number: K210195 · 2021-02-24
Device Summary
Frequently Asked Questions
What is the Triever Catheters?
Triever Catheters is a medical device that received FDA 510(k) clearance on 2021-02-24. The listed applicant is Inari Medical. The 510(k) number is K210195.
When did Triever Catheters receive FDA 510(k) clearance?
Triever Catheters received FDA 510(k) clearance on 2021-02-24, under 510(k) number K210195.
Who is the listed applicant for Triever Catheters?
The FDA 510(k) record lists Inari Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Triever Catheters?
The FDA product code for Triever Catheters is QEW.
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 Inari Medical 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.
Related Devices (Code: QEW)
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.