RIONET &/OR RION HEARING AID MODEL HA-82
K-Number: K800739 · 1980-04-24
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Device Summary
Frequently Asked Questions
What is the RIONET &/OR RION HEARING AID MODEL HA-82?
RIONET &/OR RION HEARING AID MODEL HA-82 is a medical device that received FDA 510(k) clearance on 1980-04-24. The listed applicant is Rion Acoustic Instruments, Inc.. The 510(k) number is K800739.
When did RIONET &/OR RION HEARING AID MODEL HA-82 receive FDA 510(k) clearance?
RIONET &/OR RION HEARING AID MODEL HA-82 received FDA 510(k) clearance on 1980-04-24, under 510(k) number K800739.
Who is the listed applicant for RIONET &/OR RION HEARING AID MODEL HA-82?
The FDA 510(k) record lists Rion Acoustic Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RIONET &/OR RION HEARING AID MODEL HA-82?
The FDA product code for RIONET &/OR RION HEARING AID MODEL HA-82 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 Rion Acoustic Instruments, 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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