Metavox MV-1000 Auditory Trainer

FDA 510(k) K832190 · Metavox, Inc.

Substantially Equivalent

510(k) numberK832190

Submission

Device name
Metavox MV-1000 Auditory Trainer
Applicant
Metavox, Inc.
Walker, MI, US
Received
July 8, 1983
Decision date
September 12, 1983
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
EPF – Hearing Aid, Group And Auditory Trainer
Device class
Class II (moderate risk)
Regulation
21 CFR 874.3320
Specialty
Ear, Nose, Throat

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K960567HF Mega EarEPF · Traditional Maxi-Aids, Inc.10/16/1996SE
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More from Phonic Ear, Inc.

510(k)DeviceDecision
K833152Metavox MV-1000 Hearing AidESD · Traditional 12/08/1983SE

Questions and answers

When was Metavox MV-1000 Auditory Trainer cleared by the FDA?

Metavox MV-1000 Auditory Trainer (K832190) received a 510(k) decision of Substantially Equivalent on September 12, 1983, 66 days after the submission was received.

What is the product code of K832190?

The FDA product code is EPF – Hearing Aid, Group And Auditory Trainer, a Class II (moderate risk) device regulated under 21 CFR 874.3320.