LKB 2189 ULTROPROCESSOR— 510(k) K843506

Substantially Equivalent

Lkb Instruments, Inc.

FDA 510(k) clearance K843506 for LKB 2189 ULTROPROCESSOR, Substantially Equivalent on 1984-11-30. Applicant: Lkb Instruments, Inc..

Clearance details

Applicant: Lkb Instruments, Inc.
Product code: Code IEO
Advisory panel: Pathology
Date received: 1984-09-06
Decision date: 1984-11-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code IEO

product code IEO

Injury: 326
Total: 326

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.