EDENTEC MODEL 3711 DIGITAL RECORDER— 510(k) K910870

Substantially Equivalent

Edentec Corp.

FDA 510(k) clearance K910870 for EDENTEC MODEL 3711 DIGITAL RECORDER, Substantially Equivalent on 1991-08-29. Applicant: Edentec Corp..

Clearance details

Applicant: Edentec Corp.
Product code: Code DRT
Advisory panel: Cardiovascular
Date received: 1991-03-01
Decision date: 1991-08-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Eden Prairie, MN, US

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Adverse events under product code DRT

product code DRT

Death: 4
Total: 4

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.