This page includes the latest FDA filings for Spirulina Production Facility. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3011592854 |
| FEI Number | 3010484784 |
| Name | Spirulina Production Facility |
| Owner & Operator | Advanced Breath Diagnostics, LLC |
| Contact Address | 105 Westpark Drive Suite 150 Brentwood TN 37027 US |
| Official Correspondent |
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| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 318 Seaboard Lane Suite 313 Franklin, TN 37067 US |
| Establishment Type | Manufacture Medical Device |
Device Company | Device | Date |
|---|---|---|
Spirulina Production Facility [Advanced Breath Diagnostics, LLC] | Gastric Emptying Breath Test (GEBT) | 2015-04-30 |
Spirulina Production Facility [Advanced Breath Diagnostics, LLC] | 13C-Spirulina | 2015-04-30 |
Spirulina Production Facility [Advanced Breath Diagnostics, LLC] | 13C-Spirulina Gastric Emptying Breath Test (GEBT) | 2015-04-30 |
Spirulina Production Facility [Advanced Breath Diagnostics, LLC] | 13C-Spirulina GEBT | 2015-04-30 |