This page includes the latest FDA filings for Sure Tech Diagnostic Associates Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 1938095 |
| FEI Number | 1938095 |
| Name | SURE-TECH DIAGNOSTIC ASSOCIATES, INC. |
| Owner & Operator | SURE-TECH DIAGNOSTIC ASSOCIATES, INC. |
| Contact Address | 11040 LIN VALLE DR., SUITE D -- Saint Louis MO 63123 US |
| Official Correspondent |
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| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 11040 LIN VALLE DR., SUITE D Affton, MO 63123 US |
| Establishment Type | Manufacture Medical Device |
Device Company | Device | Date |
|---|---|---|
SURE-TECH DIAGNOSTIC ASSOCIATES, INC. | KLEIHAUER-BETKE KIT | 2008-01-07 |
SURE-TECH DIAGNOSTIC ASSOCIATES, INC. | FETAL HEMOGLOBIN KIT | 2008-01-07 |
SURE-TECH DIAGNOSTIC ASSOCIATES, INC. | FETAL HEMOGLOBIN | 1989-05-17 |