TACTAID— 510(k) K830418

Name: FDA 510(k) clearance K830418
Creator: U.S. Food and Drug Administration
Published: 1983-03-10

Substantially Equivalent

Audiological Engineering Corp.

FDA 510(k) clearance K830418 for TACTAID, Substantially Equivalent on 1983-03-10. Applicant: Audiological Engineering Corp.. Device class: Unclassified.

Clearance details

Applicant: Audiological Engineering Corp.
Product code: Code LRA
Device class: Unclassified
Advisory panel: Unknown
Date received: 1983-02-08
Decision date: 1983-03-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: MD, US

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