SONOPULS 434 ULTRASOUND THERAPY EQUIPMENT— 510(k) K850640

Name: FDA 510(k) clearance K850640
Creator: U.S. Food and Drug Administration
Published: 1985-05-14

Substantially Equivalent

Fluidotherapy Corp.

FDA 510(k) clearance K850640 for SONOPULS 434 ULTRASOUND THERAPY EQUIPMENT, Substantially Equivalent on 1985-05-14. Applicant: Fluidotherapy Corp.. Device class: 2.

Clearance details

Applicant: Fluidotherapy Corp.
Product code: Code IMI
Device class: Class 2
Regulation: 21 CFR 890.5300
Advisory panel: Physical Medicine
Date received: 1985-02-19
Decision date: 1985-05-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Houston, TX, 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.