KZK
3 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Reader, Zone, Automated
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 866.2850
- Medical specialty
- Microbiology
- Flags
- Third-party review eligible
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| SIRSCAN (K991473) | Intelligence Artificielle Applications | 1999-11-23 |
| BIOMIC MICROBIOLOGY DATA MANAGEMENT SYSTEM (K944319) | Giles Scientific, Inc. | 1994-12-15 |
| BIOMIC VIDEO PLATE READER (K932122) | Giles Scientific, Inc. | 1994-03-01 |
Track KZK automatically
Every clearance here is in the API, with alerts when new ones post.