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FDA 510(k)

BUTLER ANTIBACTERIAL INTERDENTAL TOOTHBRUSH

K-Number: K974761 · 1998-06-16

Decision Date1998-06-16
Product CodeEFW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BUTLER ANTIBACTERIAL INTERDENTAL TOOTHBRUSH is the device name listed in this FDA 510(k) record. The listed applicant is John O. Butler Co.. It received FDA 510(k) clearance on 1998-06-16 under 510(k) number K974761. The device is classified under product code EFW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BUTLER ANTIBACTERIAL INTERDENTAL TOOTHBRUSH?

BUTLER ANTIBACTERIAL INTERDENTAL TOOTHBRUSH is a medical device that received FDA 510(k) clearance on 1998-06-16. The listed applicant is John O. Butler Co.. The 510(k) number is K974761.

When did BUTLER ANTIBACTERIAL INTERDENTAL TOOTHBRUSH receive FDA 510(k) clearance?

BUTLER ANTIBACTERIAL INTERDENTAL TOOTHBRUSH received FDA 510(k) clearance on 1998-06-16, under 510(k) number K974761.

Who is the listed applicant for BUTLER ANTIBACTERIAL INTERDENTAL TOOTHBRUSH?

The FDA 510(k) record lists John O. Butler Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BUTLER ANTIBACTERIAL INTERDENTAL TOOTHBRUSH?

The FDA product code for BUTLER ANTIBACTERIAL INTERDENTAL TOOTHBRUSH is EFW.

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 John O. Butler Co. 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: EFW)

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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