Elekta Instruments, Inc.
Elekta Instruments, Inc. holds FDA 510(k) medical device clearances, first cleared 1992, most recent 1999.
Top product codes for Elekta Instruments, Inc.
Recent clearances by Elekta Instruments, Inc.
- K983678 — ELEKTA ONCOLOGY SYSTEMS PRECISE TREATMENT TABLE
- K955064 — SPETZLER TI 100 ANEURYSM CLIP
- K941823 — LEKSELL NEURO GENERATOR AND ACCESSORIES
- K946165 — CMF-TITANIUM CRANIO-MAXILLO-FACIAL FRACTURE FIXATION (OSTEOSYNTHESIS) SYSTEM
- K943468 — LEKSELL SURGIPLAN
- K932261 — ES-100 ACCESSORIES
- K925360 — ES-100 POWER SYSTEM, ES-100 SERIES
- K914808 — LEKSELL GAMMAPLAN (LGP)
Data sourced from openFDA. This site is unofficial and independent of the FDA.