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FDA 510(k)

FLOSS-A-LOT

K-Number: K760571 · 1976-09-15

ApplicantE. T. Skinner
Decision Date1976-09-15
Product CodeJES
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FLOSS-A-LOT is the device name listed in this FDA 510(k) record. The listed applicant is E. T. Skinner. It received FDA 510(k) clearance on 1976-09-15 under 510(k) number K760571. 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 FLOSS-A-LOT?

FLOSS-A-LOT is a medical device that received FDA 510(k) clearance on 1976-09-15. The listed applicant is E. T. Skinner. The 510(k) number is K760571.

When did FLOSS-A-LOT receive FDA 510(k) clearance?

FLOSS-A-LOT received FDA 510(k) clearance on 1976-09-15, under 510(k) number K760571.

Who is the listed applicant for FLOSS-A-LOT?

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

What is the FDA product code for FLOSS-A-LOT?

The FDA product code for FLOSS-A-LOT 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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