ACOUSTIQ LISTENING DEVICE— 510(k) K904755

Substantially Equivalent

Krueger Laboratories

FDA 510(k) clearance K904755 for ACOUSTIQ LISTENING DEVICE, Substantially Equivalent on 1991-01-29. Applicant: Krueger Laboratories. Device class: 2.

Clearance details

Applicant: Krueger Laboratories
Product code: Code LZI
Device class: Class 2
Regulation: 21 CFR 874.3320
Advisory panel: Ear, Nose, Throat
Date received: 1990-10-19
Decision date: 1991-01-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tempe, AZ, US

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