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JOHNSON & JOHNSON EASY SLIDE DENTAL FLOSS

K951917 Class I Traditional
Decision Date
1995-05-10
Sponsor / Applicant
Johnson & Johnson Consumer Products, Inc.

Technical Specification

510(k) Submission ID K951917
Product Code JES
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6390
Decision Date 1995-05-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

JOHNSON & JOHNSON EASY SLIDE DENTAL FLOSS received FDA 510(k) clearance under submission number K951917, sponsored by Johnson & Johnson Consumer Products, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1995-05-10.

Classification & Regulation

This clearance is catalogued under FDA product code JES and 21 CFR 872.6390, within the Dental review panel as a Class I device.