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FDA 510(k)

DOCTOR KOLYNOS TOOTHBRUSH

K-Number: K882572 · 1989-04-17

Decision Date1989-04-17
Product CodeEFW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DOCTOR KOLYNOS TOOTHBRUSH is the device name listed in this FDA 510(k) record. The listed applicant is Whitehall Laboratories, Inc.. It received FDA 510(k) clearance on 1989-04-17 under 510(k) number K882572. 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 DOCTOR KOLYNOS TOOTHBRUSH?

DOCTOR KOLYNOS TOOTHBRUSH is a medical device that received FDA 510(k) clearance on 1989-04-17. The listed applicant is Whitehall Laboratories, Inc.. The 510(k) number is K882572.

When did DOCTOR KOLYNOS TOOTHBRUSH receive FDA 510(k) clearance?

DOCTOR KOLYNOS TOOTHBRUSH received FDA 510(k) clearance on 1989-04-17, under 510(k) number K882572.

Who is the listed applicant for DOCTOR KOLYNOS TOOTHBRUSH?

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

What is the FDA product code for DOCTOR KOLYNOS TOOTHBRUSH?

The FDA product code for DOCTOR KOLYNOS 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 Whitehall Laboratories, Inc. 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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