IMMULITE TURBO HCG, MODELS LSKCG1, LSKCG5— 510(k) K994085

Substantially Equivalent

Diagnostic Products Corp.

FDA 510(k) clearance K994085 for IMMULITE TURBO HCG, MODELS LSKCG1, LSKCG5, Substantially Equivalent on 2000-01-28. Applicant: Diagnostic Products Corp..

Clearance details

Applicant: Diagnostic Products Corp.
Product code: Code DHA
Advisory panel: Clinical Chemistry
Date received: 1999-12-03
Decision date: 2000-01-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Los Angeles, CA, 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.