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FDA 510(k)

TAD MODEL #9655

K-Number: K921898 · 1992-11-02

Decision Date1992-11-02
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TAD MODEL #9655 is the device name listed in this FDA 510(k) record. The listed applicant is Loric Technology. It received FDA 510(k) clearance on 1992-11-02 under 510(k) number K921898. The device is classified under product code DRS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TAD MODEL #9655?

TAD MODEL #9655 is a medical device that received FDA 510(k) clearance on 1992-11-02. The listed applicant is Loric Technology. The 510(k) number is K921898.

When did TAD MODEL #9655 receive FDA 510(k) clearance?

TAD MODEL #9655 received FDA 510(k) clearance on 1992-11-02, under 510(k) number K921898.

Who is the listed applicant for TAD MODEL #9655?

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

What is the FDA product code for TAD MODEL #9655?

The FDA product code for TAD MODEL #9655 is DRS.

Related Clinical Trials

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.

Related Devices (Code: DRS)

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.

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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