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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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