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Surgicutt Bleeding Time Device

ACCRIVA DIAGNOSTICS HOLDINGS, INC. · Model SU50I · UDI-DI 20711234304157

JCA Prescription
1
510(k) clearances
7
Adverse events
1
Recalls
4
Facilities

Description

Surgicutt Bleeding Time Device 50/box

Recalls

DateFirmReason
2013-08-22ITC-Nexus DxITC has determined that the blade in their Surgicutt with Blotting Paper (Product Code: SUB50I; Lot: AK301M) devices may be loose.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.