This page includes the latest FDA filings for Symatese Device. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
Registration Number | 3011224555 |
FEI Number | 3011224555 |
Name | Gordon MacFarlane |
Owner & Operator | SYMATESE DEVICE |
Contact Address | 135 Route Neuve IRIGNY FR-69 Rhone 69540 FR |
US Agent |
|
Registration Status | 1 |
Initial Importer | N |
Registration Expiration | 2020-04-25 |
Registration Address | 2100 Pennbrook Pkwy North Wales, PA 19454 US |
Establishment Type |
|
Device Company | Device | Date |
---|---|---|
Gordon MacFarlane [SYMATESE DEVICE] | DOLPHIN Inflation Device | 2018-08-10 |
Gordon MacFarlane [SYMATESE DEVICE] | Traumacem V+ Syringe Kit | 2017-09-26 |
Gordon MacFarlane [SYMATESE DEVICE] | D750b Guiding Kit - Mammotome | 2016-03-21 |
Gordon MacFarlane [SYMATESE DEVICE] | D750b Guiding Kit - Hologic | 2016-03-21 |
Gordon MacFarlane [SYMATESE DEVICE] | D750b Guiding Kit - BARD 7G | 2016-03-21 |
Gordon MacFarlane [SYMATESE DEVICE] | D750b Guiding Kit - BARD 10G | 2016-03-21 |
Gordon MacFarlane [SYMATESE DEVICE] | Vertecem V + Syringe kit | 2014-12-01 |
NCAGE Code | FB7S3 | SYMATESE DEVICE |
CAGE Code | FB7S3 | SYMATESE DEVICE |