Medical Device Manufacturer · US , Holliston , MA

Diamond Diagnostics, Inc. - FDA 510(k) Cleared Devices

26 submissions · 26 cleared · Since 2001

Recent clearances: SmartLyte® Plus Electrolyte Analyzer Na+/K+/Cl-/Ca++/Li+, DIAMOND DIAGNOSTICS ISE SERUM STANDARDS, DIAMOND DIAGNOSTICS ISE URINE STANDARDS, MISSION CLINICHECK ASSAYED CHEMISTRY CONTROLS, LEVEL 1, MISSION CLINICHECK ASSAYED CHEMISTRY CONTROLS LEVEL 2, MISSION C

26
Total
26
Cleared
0
Denied

Diamond Diagnostics, Inc. has 26 FDA 510(k) cleared chemistry devices. Based in Holliston, US.

Historical record: 26 cleared submissions from 2001 to 2020.

Browse the complete list of FDA 510(k) cleared chemistry devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Diamond Diagnostics, Inc.

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