JAO — Scanner, Fluorescent Class II
FDA Device Classification
Classification Details
- Product Code
- JAO
- Device Class
- Class II
- Regulation Number
- 892.1220
- Submission Type
- Review Panel
- RA
- Medical Specialty
- Radiology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K911749 | montifore medical center | L-LINEX-RAY FLUORESCENCE | August 20, 1991 |
| K900574 | abiomed | ABIOMED BODY LEAD ANALYZER MODEL 200/20 | March 15, 1990 |