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FDA 510(k)

TENTATIVE OPERATING NAME-JAZZ BAND

K-Number: K904805 · 1991-03-29

ApplicantFranklin M. Din D.M.D., P.A.
Decision Date1991-03-29
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TENTATIVE OPERATING NAME-JAZZ BAND is the device name listed in this FDA 510(k) record. The listed applicant is Franklin M. Din D.M.D., P.A.. It received FDA 510(k) clearance on 1991-03-29 under 510(k) number K904805. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TENTATIVE OPERATING NAME-JAZZ BAND?

TENTATIVE OPERATING NAME-JAZZ BAND is a medical device that received FDA 510(k) clearance on 1991-03-29. The listed applicant is Franklin M. Din D.M.D., P.A.. The 510(k) number is K904805.

When did TENTATIVE OPERATING NAME-JAZZ BAND receive FDA 510(k) clearance?

TENTATIVE OPERATING NAME-JAZZ BAND received FDA 510(k) clearance on 1991-03-29, under 510(k) number K904805.

Who is the listed applicant for TENTATIVE OPERATING NAME-JAZZ BAND?

The FDA 510(k) record lists Franklin M. Din D.M.D., P.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TENTATIVE OPERATING NAME-JAZZ BAND?

The FDA product code for TENTATIVE OPERATING NAME-JAZZ BAND is EBF.

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Related Devices (Code: EBF)

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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