SINGLE USE LEE ELECTRODE— 510(k) K913213

Substantially Equivalent

Aspen Laboratories, Inc.

FDA 510(k) clearance K913213 for SINGLE USE LEE ELECTRODE, Substantially Equivalent on 1992-02-13. Applicant: Aspen Laboratories, Inc..

Clearance details

Applicant: Aspen Laboratories, Inc.
Product code: Code HGI
Advisory panel: Obstetrics/Gynecology
Date received: 1991-07-19
Decision date: 1992-02-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Englewood, CO, US

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Adverse events under product code HGI

product code HGI

Other: 1
Total: 1

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.