KIW
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Kit, 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 |
|---|---|---|
| GIBCO MYCOTECT KIT (CATALOG NO. 189-5672) (K860695) | Gibco Laboratories Life Technologies, Inc. | 1986-03-12 |
| GIBCO MYCOTECT 189-5670 (K851275) | Gibco Laboratories Life Technologies, Inc. | 1985-06-21 |
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