ELIACHAR LARYNGEAL FOAM STENT, MODEL ELL-1— 510(k) K000154

Name: FDA 510(k) clearance K000154
Creator: U.S. Food and Drug Administration
Published: 2000-03-29

Substantially Equivalent

E. Benson Hood Lab, Inc.

FDA 510(k) clearance K000154 for ELIACHAR LARYNGEAL FOAM STENT, MODEL ELL-1, Substantially Equivalent on 2000-03-29. Applicant: E. Benson Hood Lab, Inc.. Device class: 2.

Clearance details

Applicant: E. Benson Hood Lab, Inc.
Product code: Code FWN
Device class: Class 2
Regulation: 21 CFR 874.3620
Advisory panel: Ear, Nose, Throat
Date received: 2000-01-19
Decision date: 2000-03-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pembroke, MA, US

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