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FDA 510(k)

MT10P, MT60-PP, MT60-AGC0, AND MT60

K-Number: K962847 · 1996-08-09

Decision Date1996-08-09
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

MT10P, MT60-PP, MT60-AGC0, AND MT60 is the device name listed in this FDA 510(k) record. The listed applicant is Micro-Tech Hearing Instruments. It received FDA 510(k) clearance on 1996-08-09 under 510(k) number K962847. 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 MT10P, MT60-PP, MT60-AGC0, AND MT60?

MT10P, MT60-PP, MT60-AGC0, AND MT60 is a medical device that received FDA 510(k) clearance on 1996-08-09. The listed applicant is Micro-Tech Hearing Instruments. The 510(k) number is K962847.

When did MT10P, MT60-PP, MT60-AGC0, AND MT60 receive FDA 510(k) clearance?

MT10P, MT60-PP, MT60-AGC0, AND MT60 received FDA 510(k) clearance on 1996-08-09, under 510(k) number K962847.

Who is the listed applicant for MT10P, MT60-PP, MT60-AGC0, AND MT60?

The FDA 510(k) record lists Micro-Tech Hearing Instruments as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MT10P, MT60-PP, MT60-AGC0, AND MT60?

The FDA product code for MT10P, MT60-PP, MT60-AGC0, AND MT60 is ESD.

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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