ABBOTT LIFECARE 1050 CONTROLLER— 510(k) K842080

Name: FDA 510(k) clearance K842080
Creator: U.S. Food and Drug Administration
Published: 1984-07-18

Substantially Equivalent

Abbott Laboratories

FDA 510(k) clearance K842080 for ABBOTT LIFECARE 1050 CONTROLLER, Substantially Equivalent on 1984-07-18. Applicant: Abbott Laboratories. Device class: 2.

Clearance details

Applicant: Abbott Laboratories
Product code: Code LDR
Device class: Class 2
Regulation: 21 CFR 880.5725
Advisory panel: General Hospital
Date received: 1984-05-23
Decision date: 1984-07-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Abbott Park, IL, US

Download summary PDF View on FDA.gov ↗

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