CREST TOOTHBRUSH WITH MICROSHIELD
K-Number: K973236 · 1998-03-11
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Device Summary
Frequently Asked Questions
What is the CREST TOOTHBRUSH WITH MICROSHIELD?
CREST TOOTHBRUSH WITH MICROSHIELD is a medical device that received FDA 510(k) clearance on 1998-03-11. The listed applicant is Procter & Gamble Co.. The 510(k) number is K973236.
When did CREST TOOTHBRUSH WITH MICROSHIELD receive FDA 510(k) clearance?
CREST TOOTHBRUSH WITH MICROSHIELD received FDA 510(k) clearance on 1998-03-11, under 510(k) number K973236.
Who is the listed applicant for CREST TOOTHBRUSH WITH MICROSHIELD?
The FDA 510(k) record lists Procter & Gamble Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CREST TOOTHBRUSH WITH MICROSHIELD?
The FDA product code for CREST TOOTHBRUSH WITH MICROSHIELD 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 Procter & Gamble 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
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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