Medical Device Manufacturer · US , Tucker , GA

Elekta Instruments, Inc. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1992

8

Total

8

Cleared

0

Denied

Elekta Instruments, Inc. has 8 FDA 510(k) cleared medical devices. Based in Tucker, US.

Historical record: 8 cleared submissions from 1992 to 1999.

Browse the FDA 510(k) cleared devices submitted by Elekta Instruments, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Elekta Instruments, Inc.

8 devices

1-8 of 8

Cleared Jan 15, 1999

ELEKTA ONCOLOGY SYSTEMS PRECISE TREATMENT TABLE

Radiology · 87d

Cleared Oct 17, 1996

SPETZLER TI 100 ANEURYSM CLIP

Neurology · 346d

Cleared Mar 22, 1996

LEKSELL NEURO GENERATOR AND ACCESSORIES

Neurology · 709d

Cleared May 23, 1995

CMF-TITANIUM CRANIO-MAXILLO-FACIAL FRACTURE FIXATION (OSTEOSYNTHESIS) SYSTEM

Orthopedic · 155d

Cleared Jan 20, 1995

LEKSELL SURGIPLAN

Neurology · 185d

Cleared Jan 07, 1994

ES-100 ACCESSORIES

Orthopedic · 262d

Cleared Sep 07, 1993

ES-100 POWER SYSTEM, ES-100 SERIES

General & Plastic Surgery · 320d

Cleared Jan 23, 1992

LEKSELL GAMMAPLAN (LGP)

Radiology · 90d