Fisher Scientific Co., LLC
FDA 510(k) & PMA Approved Devices — 89 products
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Total Devices89
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K930415 | MICROHEMATOCRIT ROTOR | GKG | 1993-03-23 | View |
| 510(k) | K915825 | MARATHON 6K GENERAL-PURPOSE CENTRIFUGE | GKF | 1992-03-11 | View |
| 510(k) | K915441 | MARATHON 13K/H MICROHEMATOCRIT CENTRIFUGE | GKF | 1992-01-08 | View |
| 510(k) | K890534 | MODIFIED URIQUAL(TM) URINALYSIS CONTROL LEVEL 1 | JJW | 1989-03-08 | View |
| 510(k) | K881275 | URIQUAL(TM) URINALYSIS CONTROLS (HUMAN) I & II | JJY | 1988-05-16 | View |
| 510(k) | K874054 | FISHER DIAGNOSTICS HEMATALL III LAS REAGENT | GGK | 1987-10-20 | View |
| 510(k) | K872916 | HISTOMATIC SLIDE STAINER, CODE-ON VERSION | KPA | 1987-09-14 | View |
| 510(k) | K871058 | SERACHEM LIQUID SPINAL FLUID CONTROL (HUMAN) | JJY | 1987-04-06 | View |
| 510(k) | K863224 | HEMATALL-C PLUS HEMATOLOGY CONTROLS | JPK | 1986-10-29 | View |
| 510(k) | K862318 | FISHER DIAGNOSTICS HEMATALL-C CALIBRATOR | JPK | 1986-07-10 | View |
| 510(k) | K861185 | THERACHEM-PLUS, TRI-LEVEL TDC (TM) | JJY | 1986-05-23 | View |
| 510(k) | K860919 | THERACHEM, TDC THERAPEUTIC DRUG CONTROLS | DIF | 1986-04-11 | View |
| 510(k) | K853241 | HEMATOLOGY STAIN PACK | IAF | 1985-08-19 | View |
| 510(k) | K851151 | FISHER DIAGNOSTICS KDA CALIBRATOR II | JIX | 1985-05-20 | View |
| 510(k) | K851150 | FISHER DIAGNOSTICS KDA CALIBRATOR I | JIX | 1985-05-20 | View |
| 510(k) | K850636 | SIMUTANEOUS FIXATION & DECALCIFYING SOLUTION CAL-E | KDX | 1985-03-20 | View |
| 510(k) | K844168 | AMYLASE REAGENT CS-726 | CJA | 1984-11-20 | View |
| 510(k) | K843452 | STANDARD & SOLUTIONS FOR NOVA 4 ANALYZ | JGS | 1984-09-27 | View |
| 510(k) | K840111 | TOTAL BILIRUBIN | CIG | 1984-03-19 | View |
| 510(k) | K833950 | TOTAL PROTEIN REAGENT CS-724 | CEK | 1984-01-13 | View |
No matching devices.
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