ULTRACARE(TM) AUTOMATED PATIENT ASSIST DEVICE— 510(k) K874020

Name: FDA 510(k) clearance K874020
Creator: U.S. Food and Drug Administration
Published: 1988-01-29

Substantially Equivalent

Abbott Laboratories

FDA 510(k) clearance K874020 for ULTRACARE(TM) AUTOMATED PATIENT ASSIST DEVICE, Substantially Equivalent on 1988-01-29. Applicant: Abbott Laboratories. Device class: 2.

Clearance details

Applicant: Abbott Laboratories
Product code: Code KPF
Device class: Class 2
Regulation: 21 CFR 876.5630
Advisory panel: Gastroenterology, Urology
Date received: 1987-10-02
Decision date: 1988-01-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Abbott Park, IL, US

Download summary PDF View on FDA.gov ↗

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