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FDA 510(k)

FARRORS TMJ CASSETTE HOLDER

K-Number: K813506 · 1982-01-29

ApplicantBrell Mar Products, Inc.
Decision Date1982-01-29
Product CodeKXF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FARRORS TMJ CASSETTE HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Brell Mar Products, Inc.. It received FDA 510(k) clearance on 1982-01-29 under 510(k) number K813506. The device is classified under product code KXF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FARRORS TMJ CASSETTE HOLDER?

FARRORS TMJ CASSETTE HOLDER is a medical device that received FDA 510(k) clearance on 1982-01-29. The listed applicant is Brell Mar Products, Inc.. The 510(k) number is K813506.

When did FARRORS TMJ CASSETTE HOLDER receive FDA 510(k) clearance?

FARRORS TMJ CASSETTE HOLDER received FDA 510(k) clearance on 1982-01-29, under 510(k) number K813506.

Who is the listed applicant for FARRORS TMJ CASSETTE HOLDER?

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

What is the FDA product code for FARRORS TMJ CASSETTE HOLDER?

The FDA product code for FARRORS TMJ CASSETTE HOLDER is KXF.

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Related Devices (Code: KXF)

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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