KIZ
8 FDA 510(k) clearances · Product code
21 daysmedian time to decision
106 days90th percentile
8clearances measured
FDA profile
- Official device name
- Dish, Tissue Culture
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 864.2240
- Medical specialty
- Hematology
- Flags
- GMP exempt
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| MULTIWELL CULTURE PLATE INSERTS (K890542) | Bd Becton Dickinson Vacutainer Systems Preanalytic | 1989-02-14 |
| TISSUE CULTURE DISHES (K873891) | Nunc, Inc. | 1987-11-25 |
| TISSUE CULTURE/BACTERIOLOGICAL PETRI DISHES (K871483) | Isratech Marketing Corp. | 1987-04-29 |
| CEKK-ADHESIVE MATRIX-MULTIPLE WELL PLATE CAM-PLATE (K854724) | Lifetrac, Inc. | 1985-12-13 |
| CORNING CELL WELLS-MULTIPLE WELL PLATES (K853634) | Corning Medical & Scientific | 1985-09-16 |
| REMOVAWELL TISSUE CULTURE PLATE W/LID (K821687) | Dynatech Corp. | 1982-06-24 |
| 120 WELL HISTO-PLATE (K790958) | Dynatech Laboratories, Inc. | 1979-06-28 |
| PRESSURIZER, EXETER CEMENT (K781792) | Howmedica Corp. | 1979-02-08 |
Track KIZ automatically
Every clearance here is in the API, with alerts when new ones post.