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FDA 510(k)

INNOVATIVE HEARING CORP. #IHC 1000

K-Number: K832633 · 1983-11-21

Decision Date1983-11-21
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

INNOVATIVE HEARING CORP. #IHC 1000 is the device name listed in this FDA 510(k) record. The listed applicant is Innovative Hearing Corp.. It received FDA 510(k) clearance on 1983-11-21 under 510(k) number K832633. 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 INNOVATIVE HEARING CORP. #IHC 1000?

INNOVATIVE HEARING CORP. #IHC 1000 is a medical device that received FDA 510(k) clearance on 1983-11-21. The listed applicant is Innovative Hearing Corp.. The 510(k) number is K832633.

When did INNOVATIVE HEARING CORP. #IHC 1000 receive FDA 510(k) clearance?

INNOVATIVE HEARING CORP. #IHC 1000 received FDA 510(k) clearance on 1983-11-21, under 510(k) number K832633.

Who is the listed applicant for INNOVATIVE HEARING CORP. #IHC 1000?

The FDA 510(k) record lists Innovative Hearing Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INNOVATIVE HEARING CORP. #IHC 1000?

The FDA product code for INNOVATIVE HEARING CORP. #IHC 1000 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

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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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