PDA SYSTEM— 510(k) K842522

Substantially Equivalent

Abbott Laboratories

FDA 510(k) clearance K842522 for PDA SYSTEM, Substantially Equivalent on 1984-08-02. Applicant: Abbott Laboratories. Device class: 1.

Clearance details

Applicant: Abbott Laboratories
Product code: Code JJG
Device class: Class 1
Regulation: 21 CFR 862.2140
Advisory panel: Clinical Chemistry
Date received: 1984-06-27
Decision date: 1984-08-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Abbott Park, IL, US

Download summary PDF View on FDA.gov ↗

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