This page includes the latest FDA filings for Occam Design. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3008657524 |
| FEI Number | 3008657524 |
| Name | OCCAM DESIGN |
| Owner & Operator | Occam Design |
| Contact Address | 1044 East Chestnuts St Louisville KY 40204 US |
| Official Correspondent |
|
| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 1044 East Chestnuts St Louisville, KY 40204 US |
| Establishment Type | Manufacture Medical Device for Another Party (Contract Manufacturer) |
Device Company | Device | Date |
|---|---|---|
OCCAM DESIGN | Inscope Direct Laryngoscope | 2018-01-22 |
OCCAM DESIGN | Cobralet | 2014-01-21 |
OCCAM DESIGN | Cobra Introducer | 2014-01-21 |
OCCAM DESIGN | OUCHLESS MODEL PN10114 | 2010-06-15 |