This page includes the latest FDA filings for Devicor Medical Products Inc Warehouse Distribution Center. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
Registration Number | 3010339638 |
FEI Number | 3010339638 |
Name | Devicor Medical Products, Inc. Warehouse/Distribution Center |
Owner & Operator | Devicor Medical Products, Inc. |
Contact Address | 300 E-Business Way Fifth Floor Cincinnati OH 45241 US |
Registration Status | 1 |
Initial Importer | Y |
Registration Expiration | 2020-04-25 |
Registration Address | 4750 Lake Forest Dr Ste 120 Blue Ash, OH 45242 US |
Establishment Type |
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Device Company | Device | Date |
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Devicor Medical Products, Inc. Warehouse/Distribution Center [Devicor Medical Products, Inc.] | Sentimag | 2016-12-05 |
Devicor Medical Products, Inc. Warehouse/Distribution Center [Devicor Medical Products, Inc.] | CoreVISION Digital Specimen Radiography (DSR) System | 2016-12-05 |
Devicor Medical Products, Inc. Warehouse/Distribution Center [Devicor Medical Products, Inc.] | HydroMark | 2016-06-27 |
Devicor Medical Products, Inc. Warehouse/Distribution Center [Devicor Medical Products, Inc.] | HydroMark | 2016-06-27 |
Devicor Medical Products, Inc. Warehouse/Distribution Center [Devicor Medical Products, Inc.] | HydroMark | 2016-06-10 |
Devicor Medical Products, Inc. Warehouse/Distribution Center [Devicor Medical Products, Inc.] | Mammotome revolve | 2016-03-16 |
Devicor Medical Products, Inc. Warehouse/Distribution Center [Devicor Medical Products, Inc.] | Mammotome? Hand Held System | 2010-07-30 |
Devicor Medical Products, Inc. Warehouse/Distribution Center [Devicor Medical Products, Inc.] | Mammotome? MR Biopsy System | 2010-07-30 |
Devicor Medical Products, Inc. Warehouse/Distribution Center [Devicor Medical Products, Inc.] | Mammotome? EX Hand Held System | 2010-07-30 |