TINNITUS AID, MODEL S244— 510(k) K770938

Substantially Equivalent

Vicon Instrument Co.

FDA 510(k) clearance K770938 for TINNITUS AID, MODEL S244, Substantially Equivalent on 1977-06-28. Applicant: Vicon Instrument Co.. Device class: 2.

Clearance details

Applicant: Vicon Instrument Co.
Product code: Code KLW
Device class: Class 2
Regulation: 21 CFR 874.3400
Advisory panel: Ear, Nose, Throat
Date received: 1977-05-23
Decision date: 1977-06-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: MD, US

Download summary PDF View on FDA.gov ↗

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More clearances from Vicon Instrument Co.

K811751 — FINETONE MODEL VI HEARING AID1981-07-15
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K790064 — TINNITUS DEVICES1979-02-16
K771769 — TINNITUS MASKERS, MODELS S564&S5741978-01-03
K771762 — MODULAR HEARING DEVICE, MODEL S2911977-10-04

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