KXH — Cradle, Patient, Radiologic Class I
FDA Device Classification
Classification Details
- Product Code
- KXH
- Device Class
- Class I
- Regulation Number
- 892.1830
- Submission Type
- Review Panel
- RA
- Medical Specialty
- Radiology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K122174 | ge healthcare coils (usa instruments, inc.) | PEDIATRIC POSITIONER PAD SET | November 16, 2012 |
| K953246 | octostop | OCTOROLL | September 29, 1995 |
| K930124 | octostop | VARIANT OF OCTOSTOP AND OCTOPAQUE | February 9, 1994 |
| K933134 | spectrum x-ray | SPECTRUM DG-P7000 PEDIATRIC CRADLE | October 7, 1993 |
| K930357 | octostop | ACCESSORY TO UNIVERSAL OCTOPAQUE | July 13, 1993 |
| K884292 | fischer imaging | STRETCHER TABLE | March 31, 1989 |
| K863890 | ar custom medical products | MAMM-AIRE | October 14, 1986 |
| K840463 | spectrum x-ray | DIGITAL CRADLE | February 21, 1984 |
| K813561 | spectrum x-ray | SPECTRUM PEDIATRIC CARDLE TABLE | January 29, 1982 |