Medical Device Manufacturer · IT , Milano

SENTINEL CH. SpA - FDA 510(k) Cleared Devices

12 submissions · 12 cleared · Since 2007

Total

Cleared

Denied

SENTINEL CH. SpA has 12 FDA 510(k) cleared medical devices. Based in Milano, IT.

Latest FDA clearance: May 2025. Active since 2007. Primary specialty: Chemistry.

Browse the FDA 510(k) cleared devices submitted by SENTINEL CH. SpA Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by SENTINEL CH. SpA

12 devices

1-12 of 12

SENTINEL PLASMAPROTEINS CAL 3X

K081533 · JIX

Chemistry · 23d

Cleared Jun 19, 2008

MULTIGENT CREATININE (ENZYMATIC) ASSAY

K073634 · JFY

Chemistry · 176d

Cleared Aug 02, 2007

SENTINEL LITHIUM ASSAY

K070987 · NDW

Toxicology · 118d

SENTINEL CH. SpA - FDA 510(k) Cleared Devices

FDA 510(k) cleared devices by SENTINEL CH. SpA

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