HEARTECH HFX, HEARING AID
K-Number: K870723 · 1987-03-20
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Device Summary
Frequently Asked Questions
What is the HEARTECH HFX, HEARING AID?
HEARTECH HFX, HEARING AID is a medical device that received FDA 510(k) clearance on 1987-03-20. The listed applicant is Hearing Tech, Inc.. The 510(k) number is K870723.
When did HEARTECH HFX, HEARING AID receive FDA 510(k) clearance?
HEARTECH HFX, HEARING AID received FDA 510(k) clearance on 1987-03-20, under 510(k) number K870723.
Who is the listed applicant for HEARTECH HFX, HEARING AID?
The FDA 510(k) record lists Hearing Tech, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HEARTECH HFX, HEARING AID?
The FDA product code for HEARTECH HFX, 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 Hearing Tech, 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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