FDA 510(k) Applications Submitted by TOMMI JOKINIEMI

FDA 510(k) Number Submission Date Device Name Applicant
K001439 05/08/2000 ORTHOCEPH OC100 D INSTRUMENTARIUM CORP.
K101871 07/06/2010 TRUSIGNAL SPO2 FINGERTIP SENSOR GE HEALTHCARE FINLAND OY
K992385 07/16/1999 ORTHOPANTOMOGRAPH OP100D INSTRUMENTARIUM CORP.
K002472 08/11/2000 DELTA 32 AND DELTA 32 TACT INSTRUMENTARIUM IMAGING, INC.
K093881 12/18/2009 TRUSIGNAL SPO2 FINGER SENSOR, TRUSIGNAL SPO2 EAR SENSOR, TRUSIGNAL SPO2 WRAP SENSOR GE HEALTHCARE FINLAND OY


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