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V. Mueller

STERIS CORPORATION · Model RH2010-001 · UDI-DI 10885403113710

KBA Prescription
0
510(k) clearances
1
Adverse events
0
Recalls
86
Facilities

Description

FOMON NASAL RASP FINE TEETH DOWNCUT EACH BLADE 4.2X0.7CM OVERALL LENGTH 8-1/2 inches22CM

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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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.