ADR-10600(ADR 400),10601 (ADR 300)— 510(k) K791342

Substantially Equivalent

Physio-Control Corp.

FDA 510(k) clearance K791342 for ADR-10600(ADR 400),10601 (ADR 300), Substantially Equivalent on 1979-11-16. Applicant: Physio-Control Corp..

Clearance details

Applicant: Physio-Control Corp.
Product code: Code FKX
Advisory panel: Gastroenterology, Urology
Date received: 1979-07-17
Decision date: 1979-11-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code FKX

product code FKX

Death: 501
Injury: 6,720
Malfunction: 18,508
Other: 1
Total: 25,730

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.