KJB — Apparatus, Roller Class I
FDA Device Classification
Classification Details
- Product Code
- KJB
- Device Class
- Class I
- Regulation Number
- 864.2240
- Submission Type
- Review Panel
- PA
- Medical Specialty
- Hematology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
| K881466 | cryodyne technologies | CELL-CULTURE SHAKER | April 18, 1988 |
| K872076 | corning medical and scientific | CORNING DISPOSABLE ROLLER BOTTLES | June 15, 1987 |
| K852506 | solohill engineering | BIOGLAS MICROCARRIER BEAD | July 12, 1985 |