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FDA 510(k)

CREST TOOTHBRUSH WITH MICROSHIELD

K-Number: K973236 · 1998-03-11

Decision Date1998-03-11
Product CodeEFW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CREST TOOTHBRUSH WITH MICROSHIELD is the device name listed in this FDA 510(k) record. The listed applicant is Procter & Gamble Co.. It received FDA 510(k) clearance on 1998-03-11 under 510(k) number K973236. 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 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.

View all 22 devices →

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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