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FDA 510(k) Applications Submitted by SIMON LI
FDA 510(k) Number
Submission Date
Device Name
Applicant
K080833
03/25/2008
LOVE GUARD MALE LATEX CONDOM
TIANJIN HUMAN-CARE LATEX CORPORATION
K150932
04/06/2015
Sheath Introducer
BIOTEQUE CORP.
K191556
06/12/2019
Red Dot
Behold.AI Technologies Limited
K200582
03/06/2020
Bendit2.7 Steerable Microcatheter
Bend It Technologies Ltd.
K203842
12/31/2020
Bendit21 Microcatheter
Bend It Technologies Ltd
K230980
04/05/2023
MicroMatrix« Flex
ACell, Inc.
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