METAVOX MV-1000 HEARING AID
K-Number: K833152 · 1983-12-08
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Device Summary
Frequently Asked Questions
What is the METAVOX MV-1000 HEARING AID?
METAVOX MV-1000 HEARING AID is a medical device that received FDA 510(k) clearance on 1983-12-08. The listed applicant is Metavox, Inc.. The 510(k) number is K833152.
When did METAVOX MV-1000 HEARING AID receive FDA 510(k) clearance?
METAVOX MV-1000 HEARING AID received FDA 510(k) clearance on 1983-12-08, under 510(k) number K833152.
Who is the listed applicant for METAVOX MV-1000 HEARING AID?
The FDA 510(k) record lists Metavox, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for METAVOX MV-1000 HEARING AID?
The FDA product code for METAVOX MV-1000 HEARING AID is ESD.
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 Metavox, 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: ESD)
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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