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FDA 510(k) Applications Submitted by STEPHANIE G GARTH
FDA 510(k) Number
Submission Date
Device Name
Applicant
K131992
06/28/2013
MULTICHEM P
TECHNO-PATH MANUFACTURING LTD.
K131993
06/28/2013
MULTICHEM U
TECHNO-PATH MANUFACTURING LTD.
K132091
07/08/2013
MULTICHEM IA AND IA PLUS
TECHNO-PATH MANUFACTURING LTD.
K132174
07/15/2013
MULTICHEM WBT
TECHNO-PATH MANUFACTURING LTD.
K132751
09/03/2013
MULTICHEM S PLUS / S PLUS (ASSAYED)
TECHNO-PATH MANUFACTURING LTD.
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