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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