IN-THE-EAR HEARING AID— 510(k) K875009

Name: FDA 510(k) clearance K875009
Creator: U.S. Food and Drug Administration
Published: 1988-01-07

Substantially Equivalent

House of Hearing Aids, Ltd.

FDA 510(k) clearance K875009 for IN-THE-EAR HEARING AID, Substantially Equivalent on 1988-01-07. Applicant: House of Hearing Aids, Ltd.. Device class: 1.

Clearance details

Applicant: House of Hearing Aids, Ltd.
Product code: Code ESD
Device class: Class 1
Regulation: 21 CFR 874.3300
Advisory panel: Ear, Nose, Throat
Date received: 1987-12-04
Decision date: 1988-01-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chicago, IL, US

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Data sourced from openFDA. This site is unofficial and independent of the FDA.