Biokit USA, Inc.
FDA 510(k) & PMA Approved Devices — 16 products
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Total Devices16
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K913467 | TOXOGEN | LLA | 1993-01-11 | View |
| 510(k) | K910541 | BIOKIT RPR | GMQ | 1991-10-18 | View |
| 510(k) | K904310 | RHEUMAGEN RF T-CONTROL | DHR | 1991-05-31 | View |
| 510(k) | K910539 | RHEUMAJET RF | DHR | 1991-04-05 | View |
| 510(k) | K910686 | RHEUMAJET CRP | DCN | 1991-03-19 | View |
| 510(k) | K904311 | RHEUMAGEN ASO T-CONTROL | GTQ | 1991-01-25 | View |
| 510(k) | K904312 | RHEUMAGEN CRP T-CONTROL | DCK | 1990-10-01 | View |
| 510(k) | K896433 | MODIFIED RUBAGEN | LQN | 1989-11-29 | View |
| 510(k) | K896271 | QUANTEX RF PLUS (LATEX, BUFFER STANDARD, CONTROL) | DHR | 1989-11-08 | View |
| 510(k) | K896272 | QUANTEX CRP PLUS (LATEX, BUFFER, STANDARD, CONTROL | DCN | 1989-11-08 | View |
| 510(k) | K894486 | QUANTEX ASO PLUS (LATEX,BUFFER STANDARD,CONTROL) | GTQ | 1989-10-24 | View |
| 510(k) | K893755 | RUBAGEN | LQN | 1989-08-21 | View |
| 510(k) | K874678 | I.M.N. LATEX | KTN | 1987-12-14 | View |
| 510(k) | K854991 | REUMAGEN ASL | GTQ | 1986-04-18 | View |
| 510(k) | K843741 | RPR TEST REDITEST | GMP | 1984-10-25 | View |
| 510(k) | K842256 | AS LATEX PLUS | GTQ | 1984-06-19 | View |
No matching devices.
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