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FDA 510(k)

MEMORYMATE HEARING AID WITH PMC PROGRAMMER

K-Number: K904020 · 1990-12-17

Applicant3M Company
Decision Date1990-12-17
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

MEMORYMATE HEARING AID WITH PMC PROGRAMMER is the device name listed in this FDA 510(k) record. The listed applicant is 3M Company. It received FDA 510(k) clearance on 1990-12-17 under 510(k) number K904020. 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 MEMORYMATE HEARING AID WITH PMC PROGRAMMER?

MEMORYMATE HEARING AID WITH PMC PROGRAMMER is a medical device that received FDA 510(k) clearance on 1990-12-17. The listed applicant is 3M Company. The 510(k) number is K904020.

When did MEMORYMATE HEARING AID WITH PMC PROGRAMMER receive FDA 510(k) clearance?

MEMORYMATE HEARING AID WITH PMC PROGRAMMER received FDA 510(k) clearance on 1990-12-17, under 510(k) number K904020.

Who is the listed applicant for MEMORYMATE HEARING AID WITH PMC PROGRAMMER?

The FDA 510(k) record lists 3M Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEMORYMATE HEARING AID WITH PMC PROGRAMMER?

The FDA product code for MEMORYMATE HEARING AID WITH PMC PROGRAMMER 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 3M Company 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 322 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

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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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