ACA ACETAMINOPHEN ANALYTICAL TEST PACK— 510(k) K842548

Substantially Equivalent

E.I. Dupont DE Nemours & Co., Inc.

FDA 510(k) clearance K842548 for ACA ACETAMINOPHEN ANALYTICAL TEST PACK, Substantially Equivalent on 1984-08-16. Applicant: E.I. Dupont DE Nemours & Co., Inc..

Clearance details

Applicant: E.I. Dupont DE Nemours & Co., Inc.
Product code: Code LDP
Advisory panel: Clinical Toxicology
Date received: 1984-07-02
Decision date: 1984-08-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code LDP

product code LDP

Other: 1
Total: 1

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.