FDA 510(k) Applications Submitted by JAMES BARLEY

FDA 510(k) Number Submission Date Device Name Applicant
K980087 01/09/1998 PRESDURE PRODUCTS PRESSURE PADS, MODELS P100, P110, P120, P130, P200, P210, P220, P230, P300, P310, P320, P330 PRESSURE PRODUCTS, INC.
K942747 06/10/1994 MALCOLM-LYNN(TM) EOT SUCTION REG VALVE(TM) (SRV) ) ENGINEERED ORTHOPEDIC TECHNOLOGIES, INC.
K972320 06/23/1997 BIOZ SYSTEM & BIOZ PORTABLE CARDIODYNAMICS INTERNATIONAL CORP.
K963183 08/14/1996 BIOZ SYSTEM CARDIODYNAMICS INTERNATIONAL CORP.
K945873 12/01/1994 HYPEX(TM) JET INJECTOR EQUIDYNE SYSTEMS, INC.
K024056 12/09/2002 SURESET 3.0 ML RESERVOIR, MODEL 24-103 APPLIED DIABETES RESEARCH, INCORPORATED


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