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FDA 510(k)

PHONAK MICROVOX RESONAL FM SYSTEM

K-Number: K941768 · 1994-06-24

ApplicantPhonak, Inc.
Decision Date1994-06-24
Product CodeEPF
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

PHONAK MICROVOX RESONAL FM SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Phonak, Inc.. It received FDA 510(k) clearance on 1994-06-24 under 510(k) number K941768. The device is classified under product code EPF. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHONAK MICROVOX RESONAL FM SYSTEM?

PHONAK MICROVOX RESONAL FM SYSTEM is a medical device that received FDA 510(k) clearance on 1994-06-24. The listed applicant is Phonak, Inc.. The 510(k) number is K941768.

When did PHONAK MICROVOX RESONAL FM SYSTEM receive FDA 510(k) clearance?

PHONAK MICROVOX RESONAL FM SYSTEM received FDA 510(k) clearance on 1994-06-24, under 510(k) number K941768.

Who is the listed applicant for PHONAK MICROVOX RESONAL FM SYSTEM?

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

What is the FDA product code for PHONAK MICROVOX RESONAL FM SYSTEM?

The FDA product code for PHONAK MICROVOX RESONAL FM SYSTEM is EPF.

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Other records listing Phonak, Inc. as applicant

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.

K972106PHONAK NOVO FORTE E3K972105PHONAK EPICAK972097PHONAK MICROZOOM P 2K964035PHONAK MICROLINK, PERSONAL FM RECEIVERK961653PHONAK SONA P2K961622PHONAK PICONET2 P2 AZ

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Related Devices (Code: EPF)

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.

K982683TELEX SELECT 1-40 WITH ADAPTIVE COMPRESSIONTelex Communications, Inc.K974658INFRARED GROUP AMPLIFICATION SYSTEM, INFRARED EMITTER, INFRARED BODY WORN RECEIVER, INFRARED HEADSET RECEIVER-STEREO, ITPhonic Ear, Inc.K974287FM RECEIVER - AUDITORY TRAINERPhonic Ear, Inc.K970687WILLIAMS SOUND, PERSONAL FM, HEARING HELPERWilliams Sound, LLCK970665WILLIAMS SOUND, PERSONAL FM, HEARING HELPERWilliams Sound, LLCK960567HF MEGA EARMaxi-Aids, Inc.

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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