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FDA 510(k)

EARPOPPER, MODEL EP-2000, EP-2100, EP-3000

K-Number: K073401 · 2008-03-14

ApplicantMicromedics, Inc.
Decision Date2008-03-14
Product CodeMJV
DecisionSubstantially Equivalent

Device Summary

EARPOPPER, MODEL EP-2000, EP-2100, EP-3000 is the device name listed in this FDA 510(k) record. The listed applicant is Micromedics, Inc.. It received FDA 510(k) clearance on 2008-03-14 under 510(k) number K073401. The device is classified under product code MJV. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EARPOPPER, MODEL EP-2000, EP-2100, EP-3000?

EARPOPPER, MODEL EP-2000, EP-2100, EP-3000 is a medical device that received FDA 510(k) clearance on 2008-03-14. The listed applicant is Micromedics, Inc.. The 510(k) number is K073401.

When did EARPOPPER, MODEL EP-2000, EP-2100, EP-3000 receive FDA 510(k) clearance?

EARPOPPER, MODEL EP-2000, EP-2100, EP-3000 received FDA 510(k) clearance on 2008-03-14, under 510(k) number K073401.

Who is the listed applicant for EARPOPPER, MODEL EP-2000, EP-2100, EP-3000?

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

What is the FDA product code for EARPOPPER, MODEL EP-2000, EP-2100, EP-3000?

The FDA product code for EARPOPPER, MODEL EP-2000, EP-2100, EP-3000 is MJV.

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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.

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