HEARING AID G3H & G3T
K-Number: K832129 · 1983-07-26
Advertisement
Device Summary
Frequently Asked Questions
What is the HEARING AID G3H & G3T?
HEARING AID G3H & G3T is a medical device that received FDA 510(k) clearance on 1983-07-26. The listed applicant is Widex Hearing Aid Co., Inc.. The 510(k) number is K832129.
When did HEARING AID G3H & G3T receive FDA 510(k) clearance?
HEARING AID G3H & G3T received FDA 510(k) clearance on 1983-07-26, under 510(k) number K832129.
Who is the listed applicant for HEARING AID G3H & G3T?
The FDA 510(k) record lists Widex Hearing Aid Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HEARING AID G3H & G3T?
The FDA product code for HEARING AID G3H & G3T 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 Widex Hearing Aid Co., 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.
Advertisement