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FDA 510(k)

CREST GLIDE CLINICAL GUM PROTECTION DENTAL FLOSS

K-Number: K091964 · 2009-09-24

Decision Date2009-09-24
Product CodeJES
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CREST GLIDE CLINICAL GUM PROTECTION DENTAL FLOSS 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 2009-09-24 under 510(k) number K091964. The device is classified under product code JES. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CREST GLIDE CLINICAL GUM PROTECTION DENTAL FLOSS?

CREST GLIDE CLINICAL GUM PROTECTION DENTAL FLOSS is a medical device that received FDA 510(k) clearance on 2009-09-24. The listed applicant is Procter & Gamble Co.. The 510(k) number is K091964.

When did CREST GLIDE CLINICAL GUM PROTECTION DENTAL FLOSS receive FDA 510(k) clearance?

CREST GLIDE CLINICAL GUM PROTECTION DENTAL FLOSS received FDA 510(k) clearance on 2009-09-24, under 510(k) number K091964.

Who is the listed applicant for CREST GLIDE CLINICAL GUM PROTECTION DENTAL FLOSS?

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 GLIDE CLINICAL GUM PROTECTION DENTAL FLOSS?

The FDA product code for CREST GLIDE CLINICAL GUM PROTECTION DENTAL FLOSS is JES.

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.

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Related Devices (Code: JES)

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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