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FDA 510(k)

DENTAL FLOSS TIP

K-Number: K823278 · 1982-11-22

ApplicantSanderson Creative Products Co.
Decision Date1982-11-22
Product CodeJES
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENTAL FLOSS TIP is the device name listed in this FDA 510(k) record. The listed applicant is Sanderson Creative Products Co.. It received FDA 510(k) clearance on 1982-11-22 under 510(k) number K823278. 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 DENTAL FLOSS TIP?

DENTAL FLOSS TIP is a medical device that received FDA 510(k) clearance on 1982-11-22. The listed applicant is Sanderson Creative Products Co.. The 510(k) number is K823278.

When did DENTAL FLOSS TIP receive FDA 510(k) clearance?

DENTAL FLOSS TIP received FDA 510(k) clearance on 1982-11-22, under 510(k) number K823278.

Who is the listed applicant for DENTAL FLOSS TIP?

The FDA 510(k) record lists Sanderson Creative Products Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DENTAL FLOSS TIP?

The FDA product code for DENTAL FLOSS TIP is JES.

Related Clinical Trials

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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.

K091964CREST GLIDE CLINICAL GUM PROTECTION DENTAL FLOSSProcter & Gamble Co.K964976FLOSSBRUSH WITH FLUORIDEFlossbrush Interdental Cleaner and ApplicatorK963746IDS DENTAL FLOSS WITH SODIUM FLUORIDE MICRODENT DENTAL FLOSS WITH SODIUM FLUORIDE AP-24 DENTAL FLOSS WITH SODIUM FLUORIDWhitehill Oral Technologies, Inc.K944034PERIO-MED DENTAL FLOSSWhitehill Oral Technologies, Inc.K952091VUTLER G.U.M. WITH FLUORIDEJohn O. Butler Co.K951917JOHNSON & JOHNSON EASY SLIDE DENTAL FLOSSJohnson & Johnson Consumer Products, Inc.

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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