Labsystems, Inc.
FDA 510(k) & PMA Approved Devices — 17 products
Advertisement
Total Devices17
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K923365 | TILT/REDUCED SHEAR SEMI-RECLINE SEATING SYSTEM | ITI | 1993-03-24 | View |
| 510(k) | K896474 | RESUBMITTED FECATWIN SENSITIVE - FECA-EIA | KHE | 1990-01-25 | View |
| 510(k) | K890154 | MODIFIED LABYSYSTEMS' TOXOPLASMA GONDII IGG EIA | LGD | 1989-02-07 | View |
| 510(k) | K890091 | MODIFIED LABSYSTEMS' RUBELLA IGG EIA TEST KIT | LFX | 1989-02-03 | View |
| 510(k) | K881243 | RUBELLA IGG - EIA TEST KIT NUMBER 61 07 201 | LFX | 1988-04-04 | View |
| 510(k) | K873780 | MODIFICATION RUBELLA IGM EIA TEST KIT | LFX | 1987-10-15 | View |
| 510(k) | K873583 | AUTO-EIA | JJQ | 1987-09-22 | View |
| 510(k) | K872252 | MODIFIED TOXOPLASMA GONDII IGG EIA TEST KIT | LGD | 1987-07-01 | View |
| 510(k) | K862705 | CYTOMEGALOVIRUS IGG EIA TEST KIT | GQI | 1986-10-01 | View |
| 510(k) | K862431 | RUBELLA IGM EIA TEST KIT | LFX | 1986-08-08 | View |
| 510(k) | K862216 | TOXOPLASMA GONDII IGG EIA TEST KIT (AMENDMENT) | LGD | 1986-06-30 | View |
| 510(k) | K853696 | RUBELLA IGG EIA TEST KIT | LFX | 1986-06-17 | View |
| 510(k) | K843189 | CYTOMEGALOVIRUS IGG EIA TEST KIT | GQI | 1986-01-08 | View |
| 510(k) | K842797 | TOXOPLASMA GONDII IGM EIA TEST KIT | LGD | 1984-10-17 | View |
| 510(k) | K842773 | LABSYSTEMS FP-901 CHEMISTRY ANALYZER | JJE | 1984-09-04 | View |
| 510(k) | K833829 | TOXOPLASMA GOND II IGG DIA TEST KIT | LGD | 1984-04-24 | View |
| 510(k) | K841214 | LABSYSTEMS UNISKAN | JJQ | 1984-04-13 | View |
No matching devices.
Advertisement