Elekta Instruments, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K983678 | ELEKTA ONCOLOGY SYSTEMS PRECISE TREATMENT TABLE | January 15, 1999 |
| K955064 | SPETZLER TI 100 ANEURYSM CLIP | October 17, 1996 |
| K941823 | LEKSELL NEURO GENERATOR AND ACCESSORIES | March 22, 1996 |
| K946165 | CMF-TITANIUM CRANIO-MAXILLO-FACIAL FRACTURE FIXATION (OSTEOSYNTHESIS) SYSTEM | May 23, 1995 |
| K943468 | LEKSELL SURGIPLAN | January 20, 1995 |
| K932261 | ES-100 ACCESSORIES | January 7, 1994 |
| K925360 | ES-100 POWER SYSTEM, ES-100 SERIES | September 7, 1993 |
| K914808 | LEKSELL GAMMAPLAN (LGP) | January 23, 1992 |