IMMULITE TOXOPLASMA GONDII IGG— 510(k) K950671

Substantially Equivalent

Diagnostic Products Corp.

FDA 510(k) clearance K950671 for IMMULITE TOXOPLASMA GONDII IGG, Substantially Equivalent on 1996-02-23. Applicant: Diagnostic Products Corp..

Clearance details

Applicant: Diagnostic Products Corp.
Product code: Code LGD
Advisory panel: Microbiology
Date received: 1995-02-13
Decision date: 1996-02-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Los Angeles, CA, US

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Adverse events under product code LGD

product code LGD

Malfunction: 502
Total: 502

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.