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FDA 510(k) Applications Submitted by IN-X CORP.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K984570
12/23/1998
MINOLTA PULSOX-3/MINOLTA PULSOX-3I
IN-X CORP.
K004047
12/29/2000
HOME-AWAY SYSTEM
IN-X CORP.
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