This page includes the latest FDA filings for Mary J Grove. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 9613249 |
| FEI Number | 3002987034 |
| Name | Mary J Grove |
| Owner & Operator | CORTEX TECHNOLOGY APS |
| Contact Address | Plastvaenget 9 -- HADSUND DK-81 Region Nordjylland 9560 DK |
| Official Correspondent |
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| US Agent |
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| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 275 New Darlington Rd Media, PA 19063 US |
| Establishment Type | Manufacture Medical Device |
Device Company | Device | Date |
|---|---|---|
Mary J Grove [CORTEX TECHNOLOGY APS] | DermaScan C Ultrasonic System | 2007-11-06 |
Mary J Grove [CORTEX TECHNOLOGY APS] | CryoPro Mini | 2007-11-06 |
Mary J Grove [CORTEX TECHNOLOGY APS] | CryoPro Maxi | 2007-11-06 |