Biokit USA, Inc.
16 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| TOXOGEN (K913467) | Biokit USA, Inc. | 1993-01-11 |
| BIOKIT RPR (K910541) | Biokit USA, Inc. | 1991-10-18 |
| RHEUMAGEN RF T-CONTROL (K904310) | Biokit USA, Inc. | 1991-05-31 |
| RHEUMAJET RF (K910539) | Biokit USA, Inc. | 1991-04-05 |
| RHEUMAJET CRP (K910686) | Biokit USA, Inc. | 1991-03-19 |
| RHEUMAGEN ASO T-CONTROL (K904311) | Biokit USA, Inc. | 1991-01-25 |
| RHEUMAGEN CRP T-CONTROL (K904312) | Biokit USA, Inc. | 1990-10-01 |
| MODIFIED RUBAGEN (K896433) | Biokit USA, Inc. | 1989-11-29 |
| QUANTEX RF PLUS (LATEX, BUFFER STANDARD, CONTROL) (K896271) | Biokit USA, Inc. | 1989-11-08 |
| QUANTEX CRP PLUS (LATEX, BUFFER, STANDARD, CONTROL (K896272) | Biokit USA, Inc. | 1989-11-08 |
| QUANTEX ASO PLUS (LATEX,BUFFER STANDARD,CONTROL) (K894486) | Biokit USA, Inc. | 1989-10-24 |
| RUBAGEN (K893755) | Biokit USA, Inc. | 1989-08-21 |
| I.M.N. LATEX (K874678) | Biokit USA, Inc. | 1987-12-14 |
| REUMAGEN ASL (K854991) | Biokit USA, Inc. | 1986-04-18 |
| RPR TEST REDITEST (K843741) | Biokit USA, Inc. | 1984-10-25 |
| AS LATEX PLUS (K842256) | Biokit USA, Inc. | 1984-06-19 |
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