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.. Device class: 2.

Clearance details

Applicant: Vicon Instrument Co.
Product code: Code ETS
Device class: Class 2
Regulation: 21 CFR 874.1120
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

Download summary PDF View on FDA.gov ↗

Recent devices under product code ETS

K813557 — AUDITORY STIMULATOR1982-01-19
K811772 — AUDITORY LOCALIZER1981-07-15
K811790 — OCTOTOXIC SCREENER1981-07-15
K771188 — REVERSING CLICK GENERATOR RCG61977-07-14

More clearances from Vicon Instrument Co.

K811751 — FINETONE MODEL VI HEARING AID1981-07-15
K790878 — SCREENING AUDIOMETER, HIGH FREQUENCY1979-08-03
K771769 — TINNITUS MASKERS, MODELS S564&S5741978-01-03
K771762 — MODULAR HEARING DEVICE, MODEL S2911977-10-04
K770938 — TINNITUS AID, MODEL S2441977-06-28

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