HEARING AID (ALL IN THE EAR)
K-Number: K872995 · 1987-09-16
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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 1987-09-16. The listed applicant is Sound Crafters Hearing Instruments. The 510(k) number is K872995.
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 1987-09-16, under 510(k) number K872995.
Who is the listed applicant for HEARING AID (ALL IN THE EAR)?
The FDA 510(k) record lists Sound Crafters Hearing Instruments 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.
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