5.0 MHZ CONVEX ARRAY INTRAVAGINAL TRANSDUCER— 510(k) K895647

Name: FDA 510(k) clearance K895647
Creator: U.S. Food and Drug Administration
Published: 1989-12-18

Substantially Equivalent

Advanced Technology Laboratories, Inc.

FDA 510(k) clearance K895647 for 5.0 MHZ CONVEX ARRAY INTRAVAGINAL TRANSDUCER, Substantially Equivalent on 1989-12-18. Applicant: Advanced Technology Laboratories, Inc.. Device class: 2.

Clearance details

Applicant: Advanced Technology Laboratories, Inc.
Product code: Code HGL
Device class: Class 2
Regulation: 21 CFR 884.2960
Advisory panel: Obstetrics/Gynecology
Date received: 1989-09-20
Decision date: 1989-12-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bothell, WA, US

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