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FDA 510(k)

H.A.C. MODEL-A (ALL IN THE EAR)

K-Number: K883772 · 1988-11-14

Decision Date1988-11-14
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

H.A.C. MODEL-A (ALL IN THE EAR) is the device name listed in this FDA 510(k) record. The listed applicant is Hearing Aid Crafters. It received FDA 510(k) clearance on 1988-11-14 under 510(k) number K883772. The device is classified under product code ESD. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the H.A.C. MODEL-A (ALL IN THE EAR)?

H.A.C. MODEL-A (ALL IN THE EAR) 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 K883772.

When did H.A.C. MODEL-A (ALL IN THE EAR) receive FDA 510(k) clearance?

H.A.C. MODEL-A (ALL IN THE EAR) received FDA 510(k) clearance on 1988-11-14, under 510(k) number K883772.

Who is the listed applicant for H.A.C. MODEL-A (ALL IN THE EAR)?

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-A (ALL IN THE EAR)?

The FDA product code for H.A.C. MODEL-A (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.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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