Leeco Diagnostics, Inc.
FDA 510(k) & PMA Approved Devices — 49 products
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Total Devices49
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K895765 | LEECO PREVIEW(R) EBV (EIA) | KTN | 1989-10-31 | View |
| 510(k) | K894122 | LEECO VIS-DISK STREP-A (EIA) | GTZ | 1989-08-15 | View |
| 510(k) | K891096 | VIS-DISK HCG (EIA) JPL-041M | DHA | 1989-06-16 | View |
| 510(k) | K891095 | VIS-DISK HCG (EIA) LYOPHILIZED JPL-044M | DHA | 1989-06-16 | View |
| 510(k) | K883269 | PRL-QUANT | CFT | 1988-09-13 | View |
| 510(k) | K880577 | CONCEP-7-BHCG | JHI | 1988-03-15 | View |
| 510(k) | K880069 | LEECO PREGNASTICK (EIA) CATALOG #003 | LCX | 1988-02-11 | View |
| 510(k) | K870259 | VIS-CUBE HCG (EIA) LYOPHILIZED JPL-044 | JHI | 1987-03-10 | View |
| 510(k) | K864170 | LEECO VIS-CUBE STREP A (EIA) | GTZ | 1987-02-03 | View |
| 510(k) | K863999 | VIS-CUBE PREGNANCY HOME TEST,CAT. # JPL-042 | LCX | 1987-01-09 | View |
| 510(k) | K863933 | VIS-CUBE HCG (EIA) | JHI | 1986-12-15 | View |
| 510(k) | K861354 | RIGHT-DAY OVULATION HOME TEST | CEP | 1986-09-16 | View |
| 510(k) | K861703 | LEECO CONCEP-7-BHCG (EIA) II (MODIFIED) | JHJ | 1986-07-29 | View |
| 510(k) | K860538 | RIGHT-DAY URINARY LH (EIA) | CEP | 1986-07-29 | View |
| 510(k) | K861945 | LEE-BEAD PROLACTIN (EIA) | CFT | 1986-06-13 | View |
| 510(k) | K860947 | LEECO-SCREEN, STREP A (EIA) | GTZ | 1986-05-13 | View |
| 510(k) | K860003 | LEECO TESTOSTERONE DIAGNOSTIC KIT | CDZ | 1986-03-17 | View |
| 510(k) | K854837 | LEE-BEAD BETA FSH (EIA) | CGJ | 1986-01-13 | View |
| 510(k) | K854838 | LEE-BEAD BETA LH (EIA) | CEP | 1986-01-07 | View |
| 510(k) | K853977 | BETA-TSH-IRMA | JLW | 1985-10-22 | View |
No matching devices.
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