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FDA 510(k) Applications Submitted by ALGOTEC SYSTEMS, LTD.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K980648
02/19/1998
PRO VISION
ALGOTEC SYSTEMS, LTD.
K002894
09/18/2000
MEDIPRIME
ALGOTEC SYSTEMS, LTD.
K033013
09/26/2003
MDIFICATION TO MEDIPRIME
ALGOTEC SYSTEMS, LTD.
K954678
10/10/1995
PRO VISION
ALGOTEC SYSTEMS, LTD.
K023936
11/26/2002
MODIFICATION TO MEDIPRIME
ALGOTEC SYSTEMS, LTD.
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