FISCHER/KRYSTAL THERAPEUTIC ULTRASOUND— 510(k) K861837

Name: FDA 510(k) clearance K861837
Creator: U.S. Food and Drug Administration
Published: 1986-08-07

Substantially Equivalent

Fischer Industries, Inc.

FDA 510(k) clearance K861837 for FISCHER/KRYSTAL THERAPEUTIC ULTRASOUND, Substantially Equivalent on 1986-08-07. Applicant: Fischer Industries, Inc.. Device class: 2.

Clearance details

Applicant: Fischer Industries, Inc.
Product code: Code IMG
Device class: Class 2
Regulation: 21 CFR 890.5860
Advisory panel: Physical Medicine
Date received: 1986-05-13
Decision date: 1986-08-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Geneva, IL, US

Download summary PDF View on FDA.gov ↗

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