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FDA 510(k)

HEARIT

K-Number: K934805 · 1994-02-07

ApplicantJe Liss & Co., Inc.
Decision Date1994-02-07
Product CodeLZI
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

HEARIT is the device name listed in this FDA 510(k) record. The listed applicant is Je Liss & Co., Inc.. It received FDA 510(k) clearance on 1994-02-07 under 510(k) number K934805. The device is classified under product code LZI. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEARIT?

HEARIT is a medical device that received FDA 510(k) clearance on 1994-02-07. The listed applicant is Je Liss & Co., Inc.. The 510(k) number is K934805.

When did HEARIT receive FDA 510(k) clearance?

HEARIT received FDA 510(k) clearance on 1994-02-07, under 510(k) number K934805.

Who is the listed applicant for HEARIT?

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

What is the FDA product code for HEARIT?

The FDA product code for HEARIT is LZI.

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Related Devices (Code: LZI)

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.

K043090EASYLISTENER 2 FM, RADIUM FM AND VOCALIGHT INFRARED SOUND FIELD SYSTEMSPhonic Ear, Inc.K970974WILLIAMS SOUND, PERSONAL FM SYSTEM, HEARING HELPERWilliams Sound, LLCK970340AIR CONDUCTION ASSISTIVE LISTENING DEVICE.PERSONAL AMPLIFIERBellabK954748POCKETALKER PROWilliams Sound, LLCK952057LISTENAIDER IINational Hearing Aid Dist., Inc.K904755ACOUSTIQ LISTENING DEVICEKrueger Laboratories

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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