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FDA 510(k)

CHALLENGER/CLASSIC PUSH BUTTON HANDPIECE

K-Number: K080240 · 2008-02-07

Decision Date2008-02-07
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CHALLENGER/CLASSIC PUSH BUTTON HANDPIECE is the device name listed in this FDA 510(k) record. The listed applicant is Promident, LLC. It received FDA 510(k) clearance on 2008-02-07 under 510(k) number K080240. The device is classified under product code EFB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHALLENGER/CLASSIC PUSH BUTTON HANDPIECE?

CHALLENGER/CLASSIC PUSH BUTTON HANDPIECE is a medical device that received FDA 510(k) clearance on 2008-02-07. The listed applicant is Promident, LLC. The 510(k) number is K080240.

When did CHALLENGER/CLASSIC PUSH BUTTON HANDPIECE receive FDA 510(k) clearance?

CHALLENGER/CLASSIC PUSH BUTTON HANDPIECE received FDA 510(k) clearance on 2008-02-07, under 510(k) number K080240.

Who is the listed applicant for CHALLENGER/CLASSIC PUSH BUTTON HANDPIECE?

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

What is the FDA product code for CHALLENGER/CLASSIC PUSH BUTTON HANDPIECE?

The FDA product code for CHALLENGER/CLASSIC PUSH BUTTON HANDPIECE is EFB.

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.

Other records listing Promident, LLC as applicant

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: EFB)

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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