IZG — System, X-Ray, Photofluorographic Class II
FDA Device Classification
Classification Details
- Product Code
- IZG
- Device Class
- Class II
- Regulation Number
- 892.1730
- Submission Type
- Review Panel
- RA
- Medical Specialty
- Radiology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K960082 | spinal specialties | DISCOGRAPHY KIT | March 21, 1996 |
| K960146 | ge medical systems | G.E. STERILE DISPOSABLE RADIOGRAPHIC CONTRAST TRAY | February 27, 1996 |
| K913436 | brotherston/pxi | PXI PNEUMATIC COMPRESSION PADDLE | November 5, 1992 |
| K920393 | shimadzu medical systems | MU125M MOBILE X-RAY SYSTEM | April 6, 1992 |
| K910503 | b. braun of america | DISCOGRAPHY KIT | October 7, 1991 |
| K903808 | advanced med/surg | AMSIS RDS, RADIOGRAPHIC DISCOGRAPHY KIT | January 22, 1991 |
| K892659 | oldelft corp. of america | ELECTRODELCA | November 21, 1989 |