Company ยท US
Corindus, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 2012 to 2022. Name variants (Inc, Corp, punctuation) are merged.
9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| DXX | System, Catheter Control, Steerable | 9 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jul 27, 2022 | K221464 | CorPath GRX System Corindus, Inc. | DXX |
| Dec 11, 2020 | K202275 | CorPath GRX System Corindus, Inc. | DXX |
| Mar 29, 2018 | K180517 | CorPath GRX System Corindus, Inc. | DXX |
| Mar 1, 2018 | K173806 | CorPath GRX System Corindus, Inc. | DXX |
| Feb 15, 2018 | K173288 | CorPath GRX System Corindus, Inc. | DXX |
| Oct 27, 2016 | K160121 | CorPath GRX System Corindus, Inc. | DXX |
| Mar 18, 2016 | K152999 | CorPath 200 System Corindus, Inc. | DXX |
| Oct 2, 2015 | K150892 | CorPath 200 System Corindus, Inc. | DXX |
| Jul 19, 2012 | K120834 | CORPATH 200 SYSTEM Corindus, Inc. | DXX |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||