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FDA 510(k)

I22 CITE

K-Number: K862622 · 1986-08-01

ApplicantOticon Corp.
Decision Date1986-08-01
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

I22 CITE is the device name listed in this FDA 510(k) record. The listed applicant is Oticon Corp.. It received FDA 510(k) clearance on 1986-08-01 under 510(k) number K862622. 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 I22 CITE?

I22 CITE is a medical device that received FDA 510(k) clearance on 1986-08-01. The listed applicant is Oticon Corp.. The 510(k) number is K862622.

When did I22 CITE receive FDA 510(k) clearance?

I22 CITE received FDA 510(k) clearance on 1986-08-01, under 510(k) number K862622.

Who is the listed applicant for I22 CITE?

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

What is the FDA product code for I22 CITE?

The FDA product code for I22 CITE is ESD.

Other records listing Oticon Corp. 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.

View all 57 devices →

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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