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EARPOPPER - Ep-2000

FDA 510(k)

U (US FDA 510(k))

510(k) K073401

by Micromedics, Inc.

Identifiers

510(k) Number
K073401 FDA 510(k)
FDA Product Code
MJV FDA 510(k)
Models / Variants
Ep-2000 FDA 510(k)
Ep-2100 FDA 510(k)
Ep-3000 FDA 510(k)

Classification

Device Class
U FDA 510(k)
Advisory Committee
Unknown FDA 510(k)
FDA Decision
SESE Substantially Equivalent FDA 510(k)

EARPOPPER - Ep-2000 by Micromedics, Inc. — U — FDA_510K — listed in FDA 510(k) — 3 models — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Active

FDA_510K

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Manufacturer

Manufacturer
Micromedics, Inc.

Sources (1)

  • FDA 510(k) K073401 24 fields · synced Jun 18, 2026