MODIFIED RADIUS - MODEL NUMBER MM 5000— 510(k) K871727

Name: FDA 510(k) clearance K871727
Creator: U.S. Food and Drug Administration
Published: 1987-09-30

Substantially Equivalent

Ultrasonix, Inc.

FDA 510(k) clearance K871727 for MODIFIED RADIUS - MODEL NUMBER MM 5000, Substantially Equivalent on 1987-09-30. Applicant: Ultrasonix, Inc.. Device class: 2.

Clearance details

Applicant: Ultrasonix, Inc.
Product code: Code JOP
Device class: Class 2
Regulation: 21 CFR 870.2880
Advisory panel: Cardiovascular
Date received: 1987-04-28
Decision date: 1987-09-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: N. Yonkers, NY, US

Download summary PDF View on FDA.gov ↗

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