TINNITUS DEVICES— 510(k) K790064

Substantially Equivalent

Vicon Instrument Co.

FDA 510(k) clearance K790064 for TINNITUS DEVICES, Substantially Equivalent on 1979-02-16. Applicant: Vicon Instrument Co..

Clearance details

Applicant: Vicon Instrument Co.
Product code: Code ETS
Advisory panel: Ear, Nose, Throat
Date received: 1979-01-15
Decision date: 1979-02-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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