GKB — Device, Automated Sedimentation Rate Class I
FDA Device Classification
Classification Details
- Product Code
- GKB
- Device Class
- Class I
- Regulation Number
- 864.5800
- Submission Type
- Review Panel
- HE
- Medical Specialty
- Hematology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K892522 | gespac | SR30/SR50/SR60 AUTO SEDIMENT RATE SYSTEM, MODIFIED | May 24, 1989 |
| K890503 | gespac | SR30/SR50/SR60 AUTOMATED SEDIMENTATION RATE | February 10, 1989 |