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.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact