ANNULAR ARRAY SCANHEAD— 510(k) K871856

Name: FDA 510(k) clearance K871856
Creator: U.S. Food and Drug Administration
Published: 1987-08-28

Substantially Equivalent for Some Indications

Advanced Technology Laboratories, Inc.

FDA 510(k) clearance K871856 for ANNULAR ARRAY SCANHEAD, Substantially Equivalent for Some Indications on 1987-08-28. 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: 1987-05-12
Decision date: 1987-08-28
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Bothell, WA, US

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