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FDA 510(k)

VIBRO-COM COMMUNICATOR #8827

K-Number: K813057 · 1981-12-02

ApplicantSonic Systems, Inc.
Decision Date1981-12-02
Product CodeLRA
DecisionSubstantially Equivalent

Device Summary

VIBRO-COM COMMUNICATOR #8827 is the device name listed in this FDA 510(k) record. The listed applicant is Sonic Systems, Inc.. It received FDA 510(k) clearance on 1981-12-02 under 510(k) number K813057. The device is classified under product code LRA. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIBRO-COM COMMUNICATOR #8827?

VIBRO-COM COMMUNICATOR #8827 is a medical device that received FDA 510(k) clearance on 1981-12-02. The listed applicant is Sonic Systems, Inc.. The 510(k) number is K813057.

When did VIBRO-COM COMMUNICATOR #8827 receive FDA 510(k) clearance?

VIBRO-COM COMMUNICATOR #8827 received FDA 510(k) clearance on 1981-12-02, under 510(k) number K813057.

Who is the listed applicant for VIBRO-COM COMMUNICATOR #8827?

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

What is the FDA product code for VIBRO-COM COMMUNICATOR #8827?

The FDA product code for VIBRO-COM COMMUNICATOR #8827 is LRA.

Related Clinical Trials

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Related Devices (Code: LRA)

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.

K883853ETASevrain-Tech, Inc.K862471WEARABLE TWENTY-FOUR CHANNEL VIBROTACTILE VOCODERInstitute of LogopedicsK851441TACTICON 1600MedeconK851655TEACHER TMMonargue Intl.K843433KANIEVSKI SENSORY AID OR DEVICESpectro Industries, Inc.K831501TACTIL EAREar Three Systems

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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