DOCTOR KOLYNOS TOOTHBRUSH
K-Number: K882572 · 1989-04-17
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Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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