Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Ld Technology, LLC

FDA 510(k) & PMA Approved Devices — 11 products

Total Devices11
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K200287 BP-BT KioskDXN2020-05-15 View
510(k) K200141 Oxi-W SystemMWI2020-04-27 View
510(k) K173696 TBL-ABI SystemJOM2017-12-19 View
510(k) K160956 LD-Oxi systemMWI2016-07-06 View
510(k) K131568 SUDO PATHGZO2013-06-28 View
510(k) K130056 PATIENT MONITORMWI2013-04-11 View
510(k) K113264 ELECTRO SENSOR COMPLEX SOFTWARE (ES COMPLEX SOFTWARE)DXN2012-03-02 View
510(k) K103026 ELECTRO SENSOR -BODY COMPOSITIONMNW2011-03-29 View
510(k) K102166 ELECTRO INTERSTITIAL SCANGZO2010-12-10 View
510(k) K102442 E.S.O. (ELECTRO SENSOR OXI)DQA2010-09-10 View
510(k) K083229 E.S TECK ( ELECTRO SENSOR TECK)MWI2009-02-23 View
↑