ECCOVISION ACOUSTIC DIAGNOSTIC IMAGING ACOUSTIC PHARYNGOMETER— 510(k) K011329

Name: FDA 510(k) clearance K011329
Creator: U.S. Food and Drug Administration
Published: 2002-07-26

Substantially Equivalent

E. Benson Hood Lab, Inc.

FDA 510(k) clearance K011329 for ECCOVISION ACOUSTIC DIAGNOSTIC IMAGING ACOUSTIC PHARYNGOMETER, Substantially Equivalent on 2002-07-26. Applicant: E. Benson Hood Lab, Inc.. Device class: 2.

Clearance details

Applicant: E. Benson Hood Lab, Inc.
Product code: Code BXQ
Device class: Class 2
Regulation: 21 CFR 868.1800
Advisory panel: Anesthesiology
Date received: 2001-05-01
Decision date: 2002-07-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pembroke, MA, US

Download summary PDF View on FDA.gov ↗

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