KSI — Lectins And Protectins Class II
FDA Device Classification
Classification Details
- Product Code
- KSI
- Device Class
- Class II
- Regulation Number
- 864.9550
- Submission Type
- Review Panel
- HE
- Medical Specialty
- Hematology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
| K820368 | american dade | LECTIN-A | April 14, 1982 |
| K813413 | american dade | LECTIN H | March 4, 1982 |
| K792583 | gamma biologicals | GAMMA ARACHIS HYPOGEA LECTIN | January 16, 1980 |
| K792582 | gamma biologicals | POLY-LEC SYSTEM | January 16, 1980 |