3.0 MHZ LINEAR ARRAY PROBE MODEL UST 5031— 510(k) K860313

Name: FDA 510(k) clearance K860313
Creator: U.S. Food and Drug Administration
Published: 1986-03-17

Substantially Equivalent

Johnson & Johnson Professionals, Inc.

FDA 510(k) clearance K860313 for 3.0 MHZ LINEAR ARRAY PROBE MODEL UST 5031, Substantially Equivalent on 1986-03-17. Applicant: Johnson & Johnson Professionals, Inc.. Device class: 2.

Clearance details

Applicant: Johnson & Johnson Professionals, Inc.
Product code: Code HGL
Device class: Class 2
Regulation: 21 CFR 884.2960
Advisory panel: Obstetrics/Gynecology
Date received: 1986-01-28
Decision date: 1986-03-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ramsey, NJ, US

Download summary PDF View on FDA.gov ↗

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