Diagnostic Systems Laboratories, Inc.
FDA 510(k) & PMA Approved Devices — 94 products
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Total Devices94
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K061758 | ACTIVE RENIN IRMA | CIB | 2006-07-28 | View |
| 510(k) | K020945 | AXSYM INTACT PTH, MODEL 2G06 | CEW | 2002-05-31 | View |
| 510(k) | K020128 | ACTIVE FREE BETA-HCG ELISA, MODEL DSL-10-8500 | JHI | 2002-03-01 | View |
| 510(k) | K002128 | ACTIVE INHIBIN-A ELISA, MODEL DSL-10-28100 | NDR | 2000-12-05 | View |
| 510(k) | K001086 | FREE TESTOSTERONE ENZYME IMMUNOASSAY, MODEL DSL-10-4900 | CDZ | 2000-05-18 | View |
| 510(k) | K990138 | DSL ACTIVE AFP ELISA, MODEL DSL-10-8400 | LOJ | 1999-06-21 | View |
| 510(k) | K981871 | C-REACTIVE PROTEIN ELISA, MODEL NUMBER DSL-10-42100 | DCK | 1998-11-09 | View |
| 510(k) | K973244 | ACTIVE PSA IRMA (DSL-9700) | LTJ | 1998-08-03 | View |
| 510(k) | K973243 | ACTIVE PSA ELISA (DSL-10-9700) | LTJ | 1998-08-03 | View |
| 510(k) | K981607 | ACTIVE RENIN IRMA MODEL NUMBER DSL-25100 | CIB | 1998-05-27 | View |
| 510(k) | K973514 | ACTIVE INTACT PTH | CEW | 1997-10-31 | View |
| 510(k) | K971823 | ACTIVE TESTOSTERONE EIA (DSL-10-4000) | CDZ | 1997-06-16 | View |
| 510(k) | K971270 | DSL ACTIVE T3 EIA | CDP | 1997-05-22 | View |
| 510(k) | K971269 | DSL ACTIVE T4 EIA | KLI | 1997-05-22 | View |
| 510(k) | K970915 | DSL ESTRONE-SULFATE RIA | CGF | 1997-05-16 | View |
| 510(k) | K971353 | DSL ACTIVE NON-EXTRACTION IGF-I ELISA | CFL | 1997-05-12 | View |
| 510(k) | K970701 | DSL 1900 ACTIVE HUMAN GROWTH HORMONE IRMA (DSL 1900) | CFL | 1997-04-02 | View |
| 510(k) | K962895 | DSL DHEA-S-7 | JKC | 1996-09-10 | View |
| 510(k) | K962118 | DSL ACTIVE FSH IRMA | CGJ | 1996-09-09 | View |
| 510(k) | K962758 | DSL 9100 IGF-II IRMA | CFL | 1996-08-30 | View |
No matching devices.
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