510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K072079Substantially Equivalent

Iguide System

Medical Intelligence Medizintechnik-GmbH-An Elekta, Schwabmunchen, DE / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K072079 is the FDA 510(k) clearance record for IGUIDE SYSTEM, a class II device, cleared for Medical Intelligence Medizintechnik-GmbH-An Elekta on under FDA product code IYE (Accelerator, Linear, Medical). FDA records list 3 510(k) clearances for Medical Intelligence Medizintechnik-GmbH-An Elekta, from to . As of , FDA records show 5 recalls naming K072079.

Clearance record

Decision date
Received
(15 days to decision)
Product code
IYE Accelerator, Linear, Medical
Regulation
21 CFR 892.5050
Device class
Class II
Review panel
Radiology
Applicant
Medical Intelligence Medizintechnik-GmbH-An Elekta Feyerabendstrasse 13-15, Schwabmunchen, DE
510(k) summary
Summary PDF
Third party review
Yes

Clearances, product code IYE

Trailing 12 months
16 clearances under product code IYE in the twelve months to October 2026, January 2026 the highest month at 4.
Show the numbers
Monthly 510(k) clearances under FDA product code IYE, trailing twelve months
MonthClearances
November 20251
December 20251
January 20264
February 20260
March 20261
April 20262
May 20261
June 20262
July 20260
August 20263
September 20261
October 20260