FDA 510(k) Applications Submitted by Ray Li

FDA 510(k) Number Submission Date Device Name Applicant
K220685 03/08/2022 HIGHTOP Multi-Drug Urine Test Cup, HIGHTOP Multi-Drug Urine Test Cup Rx Qingdao HIGHTOP Biotech Co., Ltd.
K961165 03/25/1996 HP M2600A OMNICARE TELEMETRY SYSTEM MODEL M2600A HEWLETT-PACKARD CO.
K030715 03/07/2003 SAFFRON NM GUIDING CATHETER NEICH MEDICAL (SHENZHEN) COMPANY LIMITED
K032888 09/16/2003 CREATION NM DIAGNOSTIC CATHETERS NEICH MEDICAL (SHENZHEN) COMPANY LIMITED


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