Beckman Instruments, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Beckman Instruments, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ACCESS TOXOPLASMA IGM REAGENTS ON THE ACCESS IMMUNOASSAY ANALYZER, MODELS 34460, 34465, 34469, ACCESS FREE T4 REAGENTS ON THE ACCESS IMMUNOASSAY ANALYZER, IMMAGE IMMUNOCHEMISTRY SYSTEM VALPROIC ACID (VPA) REAGENT
Beckman Instruments, Inc. has 281 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 281 cleared submissions from 1976 to 1998. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Beckman Instruments, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Beckman Instruments, Inc.
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