H.A.C. MODEL-B (ALL IN THE CANAL)
K-Number: K883773 · 1988-11-14
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Device Summary
Frequently Asked Questions
What is the H.A.C. MODEL-B (ALL IN THE CANAL)?
H.A.C. MODEL-B (ALL IN THE CANAL) is a medical device that received FDA 510(k) clearance on 1988-11-14. The listed applicant is Hearing Aid Crafters. The 510(k) number is K883773.
When did H.A.C. MODEL-B (ALL IN THE CANAL) receive FDA 510(k) clearance?
H.A.C. MODEL-B (ALL IN THE CANAL) received FDA 510(k) clearance on 1988-11-14, under 510(k) number K883773.
Who is the listed applicant for H.A.C. MODEL-B (ALL IN THE CANAL)?
The FDA 510(k) record lists Hearing Aid Crafters as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for H.A.C. MODEL-B (ALL IN THE CANAL)?
The FDA product code for H.A.C. MODEL-B (ALL IN THE CANAL) 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 Aid Crafters 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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