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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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