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Water Path Kit

FOCUS SURGERY INC · Model E01020AST61-I · UDI-DI 00850071153064

Prescription
0
510(k) clearances
0
Adverse events
0
Recalls
0
Facilities

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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.