ACTIVE MODEL ALP LOW PROFILE ITE HEARING AID
K-Number: K910701 · 1991-02-28
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Device Summary
Frequently Asked Questions
What is the ACTIVE MODEL ALP LOW PROFILE ITE HEARING AID?
ACTIVE MODEL ALP LOW PROFILE ITE HEARING AID is a medical device that received FDA 510(k) clearance on 1991-02-28. The listed applicant is Active Electronics, Inc.. The 510(k) number is K910701.
When did ACTIVE MODEL ALP LOW PROFILE ITE HEARING AID receive FDA 510(k) clearance?
ACTIVE MODEL ALP LOW PROFILE ITE HEARING AID received FDA 510(k) clearance on 1991-02-28, under 510(k) number K910701.
Who is the listed applicant for ACTIVE MODEL ALP LOW PROFILE ITE HEARING AID?
The FDA 510(k) record lists Active Electronics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACTIVE MODEL ALP LOW PROFILE ITE HEARING AID?
The FDA product code for ACTIVE MODEL ALP LOW PROFILE ITE 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 Active Electronics, 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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