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FDA 510(k)

FONIX TYPE 5100 HEARING AID ANALYZER

K-Number: K801905 · 1980-08-27

Decision Date1980-08-27
Product CodeETW
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

FONIX TYPE 5100 HEARING AID ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Frye Electronics, Inc.. It received FDA 510(k) clearance on 1980-08-27 under 510(k) number K801905. The device is classified under product code ETW. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FONIX TYPE 5100 HEARING AID ANALYZER?

FONIX TYPE 5100 HEARING AID ANALYZER is a medical device that received FDA 510(k) clearance on 1980-08-27. The listed applicant is Frye Electronics, Inc.. The 510(k) number is K801905.

When did FONIX TYPE 5100 HEARING AID ANALYZER receive FDA 510(k) clearance?

FONIX TYPE 5100 HEARING AID ANALYZER received FDA 510(k) clearance on 1980-08-27, under 510(k) number K801905.

Who is the listed applicant for FONIX TYPE 5100 HEARING AID ANALYZER?

The FDA 510(k) record lists Frye Electronics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FONIX TYPE 5100 HEARING AID ANALYZER?

The FDA product code for FONIX TYPE 5100 HEARING AID ANALYZER is ETW.

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 Frye Electronics, Inc. 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 13 devices →

Related Devices (Code: ETW)

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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