GROUP AUDITORY TRAINER (GROUP AMPLIFICATION SYSTEM)
K-Number: K950730 · 1995-06-30
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Device Summary
Frequently Asked Questions
What is the GROUP AUDITORY TRAINER (GROUP AMPLIFICATION SYSTEM)?
GROUP AUDITORY TRAINER (GROUP AMPLIFICATION SYSTEM) is a medical device that received FDA 510(k) clearance on 1995-06-30. The listed applicant is Phonic Ear, Inc.. The 510(k) number is K950730.
When did GROUP AUDITORY TRAINER (GROUP AMPLIFICATION SYSTEM) receive FDA 510(k) clearance?
GROUP AUDITORY TRAINER (GROUP AMPLIFICATION SYSTEM) received FDA 510(k) clearance on 1995-06-30, under 510(k) number K950730.
Who is the listed applicant for GROUP AUDITORY TRAINER (GROUP AMPLIFICATION SYSTEM)?
The FDA 510(k) record lists Phonic Ear, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GROUP AUDITORY TRAINER (GROUP AMPLIFICATION SYSTEM)?
The FDA product code for GROUP AUDITORY TRAINER (GROUP AMPLIFICATION SYSTEM) is EPF.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Phonic Ear, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: EPF)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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