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Scanditronix, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K934303RFA A-300August 9, 1994
K942092DPD-3July 29, 1994
K925133DPD-510 THERAPEUTIC RADIATION DOSIMETERJanuary 4, 1993
K914926SCANDIPLAN - VERSION 338May 28, 1992
K904753DIOLASENovember 9, 1990
K900434MM-22 MICROTRON, MM50 MICROTRONOctober 23, 1990
K843366SUPERPETTNovember 21, 1984