Medical Device
Manufacturing
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K982549Substantially Equivalent

Radionics Mini Multi-Leaf Collimator, Model Radionics Mmlc

Radionics, Inc., Burlington MA / Traditional, Substantially Equivalent

K982549 is the FDA 510(k) clearance record for RADIONICS MINI MULTI-LEAF COLLIMATOR, MODEL RADIONICS MMLC, a class II device, cleared for Radionics, Inc. on under FDA product code IYE (Accelerator, Linear, Medical). FDA records list 57 510(k) clearances for Radionics, Inc., from to . As of , FDA records show no recalls naming K982549.

Clearance record

Decision date
Received
(162 days to decision)
Product code
IYE Accelerator, Linear, Medical
Regulation
21 CFR 892.5050
Device class
Class II
Review panel
Radiology
Applicant
Radionics, Inc. 22 Terry Ave., Burlington MA
510(k) summary
Summary
Third party review
No

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