SONICATOR 710 (MODEL ME710)— 510(k) K880901

Name: FDA 510(k) clearance K880901
Creator: U.S. Food and Drug Administration
Published: 1988-03-17

Substantially Equivalent

Mettler Electronics Corp.

FDA 510(k) clearance K880901 for SONICATOR 710 (MODEL ME710), Substantially Equivalent on 1988-03-17. Applicant: Mettler Electronics Corp.. Device class: 2.

Clearance details

Applicant: Mettler Electronics Corp.
Product code: Code IMI
Device class: Class 2
Regulation: 21 CFR 890.5300
Advisory panel: Physical Medicine
Date received: 1988-03-02
Decision date: 1988-03-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Anaheim, CA, 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.