TDX REA BUN— 510(k) K853677

Substantially Equivalent

Abbott Laboratories

FDA 510(k) clearance K853677 for TDX REA BUN, Substantially Equivalent on 1985-09-16. Applicant: Abbott Laboratories. Device class: 2.

Clearance details

Applicant: Abbott Laboratories
Product code: Code CDQ
Device class: Class 2
Regulation: 21 CFR 862.1770
Advisory panel: Clinical Chemistry
Date received: 1985-09-04
Decision date: 1985-09-16
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.