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FDA 510(k)

BUFFING FLOSS

K-Number: K911470 · 1991-05-15

ApplicantLamar Industries
Decision Date1991-05-15
Product CodeJES
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BUFFING FLOSS is the device name listed in this FDA 510(k) record. The listed applicant is Lamar Industries. It received FDA 510(k) clearance on 1991-05-15 under 510(k) number K911470. 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 BUFFING FLOSS?

BUFFING FLOSS is a medical device that received FDA 510(k) clearance on 1991-05-15. The listed applicant is Lamar Industries. The 510(k) number is K911470.

When did BUFFING FLOSS receive FDA 510(k) clearance?

BUFFING FLOSS received FDA 510(k) clearance on 1991-05-15, under 510(k) number K911470.

Who is the listed applicant for BUFFING FLOSS?

The FDA 510(k) record lists Lamar Industries as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BUFFING FLOSS?

The FDA product code for BUFFING FLOSS is JES.

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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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