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FDA 510(k)

EARCLEAR

K-Number: K951596 · 1995-05-24

ApplicantArisil Medical
Decision Date1995-05-24
Product CodeMJV
DecisionSubstantially Equivalent

Device Summary

EARCLEAR is the device name listed in this FDA 510(k) record. The listed applicant is Arisil Medical. It received FDA 510(k) clearance on 1995-05-24 under 510(k) number K951596. The device is classified under product code MJV. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EARCLEAR?

EARCLEAR is a medical device that received FDA 510(k) clearance on 1995-05-24. The listed applicant is Arisil Medical. The 510(k) number is K951596.

When did EARCLEAR receive FDA 510(k) clearance?

EARCLEAR received FDA 510(k) clearance on 1995-05-24, under 510(k) number K951596.

Who is the listed applicant for EARCLEAR?

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

What is the FDA product code for EARCLEAR?

The FDA product code for EARCLEAR is MJV.

Related Clinical Trials

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Related Devices (Code: MJV)

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.

K252751Earflo (EF001)Earflo, Inc.K230502Ear Pressure Relief Device(Model:ER813B)Ningbo Albert Novosino Co., Ltd.K203754Eustachi Ear Pressure Relief DeviceExercore, LLCK073401EARPOPPER, MODEL EP-2000, EP-2100, EP-3000Micromedics, Inc.K920840OTOVENTAbigo Medical AB

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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