EDENTEC MULTI-CHANNEL RECORDER— 510(k) K873081

Substantially Equivalent

Edentec Corp.

FDA 510(k) clearance K873081 for EDENTEC MULTI-CHANNEL RECORDER, Substantially Equivalent on 1987-11-17. Applicant: Edentec Corp..

Clearance details

Applicant: Edentec Corp.
Product code: Code DQA
Advisory panel: Cardiovascular
Date received: 1987-08-05
Decision date: 1987-11-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Eden Prairie, MN, US

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Adverse events under product code DQA

product code DQA

Death: 66
Malfunction: 2,867
Other: 1
Total: 2,934

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.