Gds Technology, LLC
FDA 510(k) & PMA Approved Devices — 7 products
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Total Devices7
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K994073 | HEMOSITE TEST SYSTEM | KHG | 2000-01-14 | View |
| 510(k) | K992132 | CHOLESITE TEST SYSTEM | CHH | 1999-08-20 | View |
| 510(k) | K973649 | HEMOSITE TEST SYSTEM | KHG | 1998-08-31 | View |
| 510(k) | K971145 | GLUCOSITE TEST SYSTEM | CGA | 1997-09-17 | View |
| 510(k) | K911801 | KETOSITE(TM)/STAT-SITE(TM)/KETOSITE(TM) LOW-HI CON | JIN | 1991-07-01 | View |
| 510(k) | K882038 | GDS ENZYMATIC SALICYLATE REAGENT | DKJ | 1988-06-24 | View |
| 510(k) | K880829 | GDS ENZYMATIC ACETAMINOPHEN REAGENT | LDP | 1988-05-27 | View |
No matching devices.
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