CHRONODYNAMICS DATA RECORDER (CDR)-100— 510(k) K881813

Substantially Equivalent

Chronodynamics, Inc.

FDA 510(k) clearance K881813 for CHRONODYNAMICS DATA RECORDER (CDR)-100, Substantially Equivalent on 1988-12-05. Applicant: Chronodynamics, Inc..

Clearance details

Applicant: Chronodynamics, Inc.
Product code: Code FLL
Advisory panel: General Hospital
Date received: 1988-04-28
Decision date: 1988-12-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Dayton, OH, US

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Adverse events under product code FLL

product code FLL

Death: 3
Malfunction: 557
Total: 560

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.