IMMULITE FREE T3— 510(k) K974634

Substantially Equivalent

Diagnostic Products Corp.

FDA 510(k) clearance K974634 for IMMULITE FREE T3, Substantially Equivalent on 1998-01-02. Applicant: Diagnostic Products Corp.. Device class: 2.

Clearance details

Applicant
Diagnostic Products Corp.
Product code
Code CDP
Device class
Class 2
Regulation
21 CFR 862.1710
Advisory panel
Clinical Chemistry
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Los Angeles, CA, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code CDP

product code CDP
Malfunction
647
Total
647

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Recalls naming K974634

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K974634.

Data sourced from openFDA. This site is unofficial and independent of the FDA.