LODE COAGULOMETER MODEL LC-6— 510(k) K852450

Substantially Equivalent

Lode Corp.

FDA 510(k) clearance K852450 for LODE COAGULOMETER MODEL LC-6, Substantially Equivalent on 1985-09-30. Applicant: Lode Corp..

Clearance details

Applicant: Lode Corp.
Product code: Code JPA
Advisory panel: Hematology
Date received: 1985-06-10
Decision date: 1985-09-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Seattle, WA, US

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Adverse events under product code JPA

product code JPA

Death: 6
Total: 6

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.