RESUBMITTED ABBOTT TESTPACK(TM) HCG COMBO— 510(k) K884207

Substantially Equivalent

Abbott Laboratories

FDA 510(k) clearance K884207 for RESUBMITTED ABBOTT TESTPACK(TM) HCG COMBO, Substantially Equivalent on 1988-12-02. Applicant: Abbott Laboratories.

Clearance details

Applicant: Abbott Laboratories
Product code: Code DHA
Advisory panel: Clinical Chemistry
Date received: 1988-10-06
Decision date: 1988-12-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Abbott Park, IL, 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.