ELMED

ELMED INCORPORATED · Model 5984 · UDI-DI 00842180106802

BWA Prescription

510(k) clearances

Adverse events

Recalls

Facilities

Description

"ELMED SYSTEM FOR BIPOLAR SUBMUCOSAL TURBINATE SURGERY CONSISTING OF: LIST NO. 5300 ELMED BC 50 M/M GENERATOR, LIST NO. 5970 DENNIS TURBINATE PROBE, LIST NO. 5707 FOOTSWITCH, LIST NO. 5302 BIPOLAR RF-CABLE, LIST NO. 55200-03 STERILIZATION AND STORAGE CASE AND LIST NO. 5975 INSTRUCTIONAL VIDEO TAPE"

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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.