DIAGNOSTIC ULTRASOUND 105 & 110— 510(k) K842539

Name: FDA 510(k) clearance K842539
Creator: U.S. Food and Drug Administration
Published: 1985-04-10

Substantially Equivalent

Diagnostic Ultrasound Corp.

FDA 510(k) clearance K842539 for DIAGNOSTIC ULTRASOUND 105 & 110, Substantially Equivalent on 1985-04-10. Applicant: Diagnostic Ultrasound Corp.. Device class: 2.

Clearance details

Applicant: Diagnostic Ultrasound Corp.
Product code: Code JOP
Device class: Class 2
Regulation: 21 CFR 870.2880
Advisory panel: Cardiovascular
Date received: 1984-06-28
Decision date: 1985-04-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kirkland, WA, US

Download summary PDF View on FDA.gov ↗

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