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FDA 510(k) Applications Submitted by POLLOGEN LTD
FDA 510(k) Number
Submission Date
Device Name
Applicant
K140255
01/31/2014
STOP U (PACKED BLACK USA); STOP U (PACKED WHITE USA)
POLLOGEN LTD
K131758
06/17/2013
SURGEN U
POLLOGEN LTD
K111026
04/13/2011
APOLLO
POLLOGEN LTD
K122200
07/25/2012
A3F FRATIONAL
POLLOGEN LTD
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