KPB
4 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Media And Components, Mycoplasma Detection
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 864.2360
- Medical specialty
- Hematology
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| STAIN KIT FOR CELL CULTURES (30-100-00) (K781875) | Flow Laboratories, Inc. | 1978-12-20 |
| MYCOPLASMA ARGININI FITC (30-403-41) (K781874) | Flow Laboratories, Inc. | 1978-12-20 |
| MYCOPLASMA HYORHINIS (BTS-7) (K781390) | Flow Laboratories, Inc. | 1978-09-01 |
| MYCOPLASMA DETECTION KIT (K771867) | Bioassay Systems Research Corp. | 1977-11-17 |
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