KZK — Reader, Zone, Automated Class I
FDA Device Classification
Classification Details
- Product Code
- KZK
- Device Class
- Class I
- Regulation Number
- 866.2850
- Submission Type
- Review Panel
- MI
- Medical Specialty
- Microbiology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K991473 | intelligence artificielle applications | SIRSCAN | November 23, 1999 |
| K944319 | giles scientific | BIOMIC MICROBIOLOGY DATA MANAGEMENT SYSTEM | December 15, 1994 |
| K932122 | giles scientific | BIOMIC VIDEO PLATE READER | March 1, 1994 |