OMNICOR PROGRAMMER MODEL 222C— 510(k) K791419

Substantially Equivalent

Cordis Corp.

FDA 510(k) clearance K791419 for OMNICOR PROGRAMMER MODEL 222C, Substantially Equivalent on 1979-11-27. Applicant: Cordis Corp..

Clearance details

Applicant: Cordis Corp.
Product code: Code KRG
Advisory panel: Cardiovascular
Date received: 1979-07-17
Decision date: 1979-11-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code KRG

product code KRG

Malfunction: 8,377
Total: 8,377

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.