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Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K232971

APRO 55 Catheter and Alembic Aspiration Tubing · Alembic, LLC · decided 2024-02-29 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
APRO 55 CatheterAPRO-55-125Alembic, LLCNRY00850014025250
APRO 55 CatheterAPRO-55-137Alembic, LLCNRY00850014025052