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Instrumentarium Imaging, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
24
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K002472DELTA 32 AND DELTA 32 TACTNovember 29, 2000
K001928SIGMAAugust 2, 2000
K000976DIAMOND (MAMMOGRAPHIC X-RAY SYSTEM)June 1, 2000
K001171DELTA 16 TACTMay 12, 2000
K973642ORTHOPANTOMOGRAPH OP100 AND ORTHOCEPH OC100November 21, 1997
K955411DELTA 16March 21, 1996
K925987INSTRUMENTARIUM MEGA4 HTMay 19, 1993
K924921INSTRUMENTARIUM MEGA4 HTMay 17, 1993
K924472INSTRUMENTARIUM MEGA4 HTMay 3, 1993
K923581INSTRUMENTARIUM MEGA4 HTMay 3, 1993
K923352INSTRUMENTARIUM MEGA4 HTOctober 6, 1992
K923022INSTRUMENTARIUM MEGA4 HTSeptember 22, 1992
K920215INSTRUMENTARIUM MEGA4 HTApril 14, 1992
K915552INSTRUMENTARIUM MEGA4February 27, 1992
K912180MODEL MGB-301 DIAPHRAGM FILM 24 X 30 CMOctober 21, 1991
K912963INSTRUMENTARIUM MEGA4September 30, 1991
K910111VARIOUS MODELS OF DAYLIGHT CASSETTE HOLDERSSeptember 23, 1991
K896596ALPHA III PLUS AND MODEL P2500F/101 W/OPTIONALMay 30, 1991
K904528INSTRUMENTARIUM MEGA4, MODIFICATIONNovember 20, 1990
K902044MEGA 4 MAGNETIC RESONANCE IMAGING SYSTEMAugust 23, 1990