This page includes the latest FDA filings for Catheter Precision Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3010728615 |
| FEI Number | 3010728615 |
| Name | Catheter Precision, Incorporated |
| Owner & Operator | Catheter Precision |
| Contact Address | 500 International Drive Suite 333 Mount Olive NJ 07828 US |
| Official Correspondent |
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| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 500 International Drive Suite 255 Mount Olive, NJ 07828 US |
| Establishment Type | Manufacture Medical Device |
Device Company | Device | Date |
|---|---|---|
Catheter Precision, Inc. | VIVO | 2020-09-14 |
Catheter Precision, Incorporated [Catheter Precision] | VIVO | 2019-09-09 |
Catheter Precision, Inc. | VIVO | 2019-06-14 |