Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

EARETTE HEARING AID OTICON E30V

K-Number: K842074 · 1984-08-23

ApplicantOticon Corp.
Decision Date1984-08-23
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

EARETTE HEARING AID OTICON E30V is the device name listed in this FDA 510(k) record. The listed applicant is Oticon Corp.. It received FDA 510(k) clearance on 1984-08-23 under 510(k) number K842074. 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 EARETTE HEARING AID OTICON E30V?

EARETTE HEARING AID OTICON E30V is a medical device that received FDA 510(k) clearance on 1984-08-23. The listed applicant is Oticon Corp.. The 510(k) number is K842074.

When did EARETTE HEARING AID OTICON E30V receive FDA 510(k) clearance?

EARETTE HEARING AID OTICON E30V received FDA 510(k) clearance on 1984-08-23, under 510(k) number K842074.

Who is the listed applicant for EARETTE HEARING AID OTICON E30V?

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 EARETTE HEARING AID OTICON E30V?

The FDA product code for EARETTE HEARING AID OTICON E30V 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 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.

↑