VIS-DISK HCG (EIA) JPL-041M— 510(k) K891096

Substantially Equivalent

Leeco Diagnostics, Inc.

FDA 510(k) clearance K891096 for VIS-DISK HCG (EIA) JPL-041M, Substantially Equivalent on 1989-06-16. Applicant: Leeco Diagnostics, Inc..

Clearance details

Applicant: Leeco Diagnostics, Inc.
Product code: Code DHA
Advisory panel: Clinical Chemistry
Date received: 1989-03-02
Decision date: 1989-06-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Southfield, MI, US

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Adverse events under product code DHA

product code DHA

Malfunction: 1,242
Total: 1,242

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.