THE HAYEK OSCILLATOR— 510(k) K903745

Name: FDA 510(k) clearance K903745
Creator: U.S. Food and Drug Administration
Published: 1990-11-09

Substantially Equivalent

Flexco Medical Instruments

FDA 510(k) clearance K903745 for THE HAYEK OSCILLATOR, Substantially Equivalent on 1990-11-09. Applicant: Flexco Medical Instruments. Device class: 2.

Clearance details

Applicant: Flexco Medical Instruments
Product code: Code BYT
Device class: Class 2
Regulation: 21 CFR 868.5935
Advisory panel: Anesthesiology
Date received: 1990-08-16
Decision date: 1990-11-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Zurich, Switzerland, CH

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