AHS OMEGA HF
K-Number: K963878 · 1996-12-06
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Device Summary
Frequently Asked Questions
What is the AHS OMEGA HF?
AHS OMEGA HF is a medical device that received FDA 510(k) clearance on 1996-12-06. The listed applicant is Authorized Hearing Systems, Inc.. The 510(k) number is K963878.
When did AHS OMEGA HF receive FDA 510(k) clearance?
AHS OMEGA HF received FDA 510(k) clearance on 1996-12-06, under 510(k) number K963878.
Who is the listed applicant for AHS OMEGA HF?
The FDA 510(k) record lists Authorized Hearing Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AHS OMEGA HF?
The FDA product code for AHS OMEGA HF 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 Authorized Hearing Systems, 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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