KRONNER SIDE-KICK UTERINE MANIPULATOR HOLDER— 510(k) K130758

Substantially Equivalent

Kronner Prototypes, Inc.

FDA 510(k) clearance K130758 for KRONNER SIDE-KICK UTERINE MANIPULATOR HOLDER, Substantially Equivalent on 2013-12-11. Applicant: Kronner Prototypes, Inc..

Clearance details

Applicant: Kronner Prototypes, Inc.
Product code: Code LKF
Advisory panel: Obstetrics/Gynecology
Date received: 2013-03-20
Decision date: 2013-12-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Roseburg, OR, US

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Adverse events under product code LKF

product code LKF

Malfunction: 643
Other: 2
Total: 645

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.