FDA 510(k)

RADIOEAR MODEL 1072

K-Number: K770402 · 1977-03-10

Decision Date1977-03-10

Product Code

DecisionSubstantially Equivalent

Device Summary

RADIOEAR MODEL 1072 is the device name listed in this FDA 510(k) record. The listed applicant is Radioear Corp.. It received FDA 510(k) clearance on 1977-03-10 under 510(k) number K770402. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RADIOEAR MODEL 1072?

RADIOEAR MODEL 1072 is a medical device that received FDA 510(k) clearance on 1977-03-10. The listed applicant is Radioear Corp.. The 510(k) number is K770402.

When did RADIOEAR MODEL 1072 receive FDA 510(k) clearance?

RADIOEAR MODEL 1072 received FDA 510(k) clearance on 1977-03-10, under 510(k) number K770402.

Who is the listed applicant for RADIOEAR MODEL 1072?

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

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Other records listing Radioear Corp. as applicant

K841934RADIOEAR M430 PP K841933RADIOEAR M420H K841473HEARING AID MODEL 440PPC K841475HEARING AID MODEL M400 K841474HEARING AID MODEL P500 K834523MODEL M410D HEARING AID

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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.