This page includes the latest FDA filings for Kathleen Chester. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3011215818 |
| FEI Number | 3011215818 |
| Name | Kathleen Chester |
| Owner & Operator | HOLOGIC, INC. |
| Contact Address | 250 Campus Drive -- Marlborough MA 01752 US |
| US Agent |
|
| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 10210 Genetic Center Drive -- San Diego, CA 92121 US |
| Establishment Type | Manufacture Medical Device for Another Party (Contract Manufacturer) |
Device Company | Device | Date |
|---|---|---|
Kathleen Chester [HOLOGIC, INC.] | Aptima Mycoplasma genitalium Calibrators Kit | 2019-01-23 |
Kathleen Chester [HOLOGIC, INC.] | Aptima Mycoplasma genitalium Assay | 2019-01-23 |