HEARING AID (ALL-IN-THE-EAR)
K-Number: K930542 · 1993-04-07
Advertisement
Device Summary
Frequently Asked Questions
What is the HEARING AID (ALL-IN-THE-EAR)?
HEARING AID (ALL-IN-THE-EAR) is a medical device that received FDA 510(k) clearance on 1993-04-07. The listed applicant is Action Labs, Inc.. The 510(k) number is K930542.
When did HEARING AID (ALL-IN-THE-EAR) receive FDA 510(k) clearance?
HEARING AID (ALL-IN-THE-EAR) received FDA 510(k) clearance on 1993-04-07, under 510(k) number K930542.
Who is the listed applicant for HEARING AID (ALL-IN-THE-EAR)?
The FDA 510(k) record lists Action Labs, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HEARING AID (ALL-IN-THE-EAR)?
The FDA product code for HEARING AID (ALL-IN-THE-EAR) 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.
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