JEDMED LARYNGEAL SCOPE— 510(k) K950925

Substantially Equivalent

Jedmed Instrument Co.

FDA 510(k) clearance K950925 for JEDMED LARYNGEAL SCOPE, Substantially Equivalent on 1995-08-11. Applicant: Jedmed Instrument Co..

Clearance details

Applicant: Jedmed Instrument Co.
Product code: Code EOQ
Advisory panel: Ear, Nose, Throat
Date received: 1995-03-01
Decision date: 1995-08-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St.Louis, MO, US

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Adverse events under product code EOQ

product code EOQ

Death: 135
Injury: 2,863
Malfunction: 21,662
Total: 24,660

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.