MEERCI RETRIEVER, CONCENTRIC MICROCATHETER, MODELS 90050, 90060, 90065, 90066, 90070,90092, 90043, 90044— 510(k) K072796

Clearance details

Applicant

Concentric Medical, Inc.

Product code

Code DQO

Device class

Class 2

Regulation

21 CFR 870.1200

Advisory panel

Cardiovascular

Date received

2007-10-01

Decision date

2007-12-18

Decision

Substantially Equivalent

Clearance type

Special

Location

Mountain View, CA, US

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• K254278 — Arterial Pressure Monitoring Set/Tray2026-03-25
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• K173352 — Trevo Pro Vue Retriever and Trevo XP Pro Vue Retriever (Trevo Retriever)2018-02-15
• DEN150049 — Modified Trevo ProVue Retriever, Trevo XP ProVue Retriever 4x20mm, Trevo XP ProVue Retriever 3x20mm, Trevo XP ProVue Retriever 6x25mm, Trevo XP ProVue Retriever 4x30mm2016-09-02
• K150616 — Trevo XP ProVue Retriever (4x30mm)2015-06-12
• K143077 — Trevo XP ProVue Retriever (6X25mm)2015-04-06
• K133177 — MODIFIED HD GUIDE CATHETER2014-02-25

Death

35

Injury

993

Malfunction

1,772

Other

5

Total

2,805

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →