AUTOMATED MEDICAL REPORT WRITER— 510(k) K981553

Name: FDA 510(k) clearance K981553
Creator: U.S. Food and Drug Administration
Published: 1998-09-29

Substantially Equivalent

Woodson and Associates, LLC

FDA 510(k) clearance K981553 for AUTOMATED MEDICAL REPORT WRITER, Substantially Equivalent on 1998-09-29. Applicant: Woodson and Associates, LLC. Device class: 2.

Clearance details

Applicant: Woodson and Associates, LLC
Product code: Code KPS
Device class: Class 2
Regulation: 21 CFR 892.1200
Advisory panel: Radiology
Date received: 1998-05-01
Decision date: 1998-09-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Decatur, GA, US

Download summary PDF View on FDA.gov ↗

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