MEMORYMATE HEARING AID MODEL 8200
K-Number: K880082 · 1988-03-09
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Device Summary
Frequently Asked Questions
What is the MEMORYMATE HEARING AID MODEL 8200?
MEMORYMATE HEARING AID MODEL 8200 is a medical device that received FDA 510(k) clearance on 1988-03-09. The listed applicant is 3M Company. The 510(k) number is K880082.
When did MEMORYMATE HEARING AID MODEL 8200 receive FDA 510(k) clearance?
MEMORYMATE HEARING AID MODEL 8200 received FDA 510(k) clearance on 1988-03-09, under 510(k) number K880082.
Who is the listed applicant for MEMORYMATE HEARING AID MODEL 8200?
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 MODEL 8200?
The FDA product code for MEMORYMATE HEARING AID MODEL 8200 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.
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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