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ELMED

ELMED INCORPORATED · Model 9820PA · UDI-DI 00198506058905

EQH Prescription
10
510(k) clearances
36
Adverse events
1
Recalls
99
Facilities

Description

FIBEROPTIC CABLE WITH UNIVERSAL SCOPE & LIGHT SOURCE CONNECTORS (PILLING SCOPE & ACMI LIGHT SOURCE), NON-RETURNABLE

Recalls

DateFirmReason
2007-02-07Boston Scientific CorporationLight Degradation in transmission-A film may deposit on the front face and limit transmission of light

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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.