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FDA 510(k)

THE COMMUNICATOR

K-Number: K821677 · 1982-06-22

ApplicantRobert Swinney. , Ltd.
Decision Date1982-06-22
Product CodeILQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

THE COMMUNICATOR is the device name listed in this FDA 510(k) record. The listed applicant is Robert Swinney. , Ltd.. It received FDA 510(k) clearance on 1982-06-22 under 510(k) number K821677. The device is classified under product code ILQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE COMMUNICATOR?

THE COMMUNICATOR is a medical device that received FDA 510(k) clearance on 1982-06-22. The listed applicant is Robert Swinney. , Ltd.. The 510(k) number is K821677.

When did THE COMMUNICATOR receive FDA 510(k) clearance?

THE COMMUNICATOR received FDA 510(k) clearance on 1982-06-22, under 510(k) number K821677.

Who is the listed applicant for THE COMMUNICATOR?

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

What is the FDA product code for THE COMMUNICATOR?

The FDA product code for THE COMMUNICATOR is ILQ.

Related Clinical Trials

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Related Devices (Code: ILQ)

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.

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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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