IMMULITE ACTH CONTROL MODULE (LACCM)— 510(k) K963240

Substantially Equivalent

Diagnostic Products Corp.

FDA 510(k) clearance K963240 for IMMULITE ACTH CONTROL MODULE (LACCM), Substantially Equivalent on 1996-08-29. Applicant: Diagnostic Products Corp..

Clearance details

Applicant: Diagnostic Products Corp.
Product code: Code JJX
Advisory panel: Clinical Chemistry
Date received: 1996-08-19
Decision date: 1996-08-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Los Angeles, CA, US

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Adverse events under product code JJX

product code JJX

Other: 2
Total: 2

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.