JANACEK TUBO-UTERINE IMPLANTATION SET— 510(k) K840766

Substantially Equivalent

Cimed Intl., Inc.

FDA 510(k) clearance K840766 for JANACEK TUBO-UTERINE IMPLANTATION SET, Substantially Equivalent on 1984-04-23. Applicant: Cimed Intl., Inc..

Clearance details

Applicant: Cimed Intl., Inc.
Product code: Code HTD
Advisory panel: General, Plastic Surgery
Date received: 1984-02-23
Decision date: 1984-04-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kansas City, MO, US

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Adverse events under product code HTD

product code HTD

Malfunction: 892
Total: 892

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.