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FDA 510(k)

JOHNSON & JOHNSON EASY SLIDE DENTAL FLOSS

K-Number: K951917 · 1995-05-10

Decision Date1995-05-10
Product CodeJES
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

JOHNSON & JOHNSON EASY SLIDE DENTAL FLOSS is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Consumer Products, Inc.. It received FDA 510(k) clearance on 1995-05-10 under 510(k) number K951917. 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 JOHNSON & JOHNSON EASY SLIDE DENTAL FLOSS?

JOHNSON & JOHNSON EASY SLIDE DENTAL FLOSS is a medical device that received FDA 510(k) clearance on 1995-05-10. The listed applicant is Johnson & Johnson Consumer Products, Inc.. The 510(k) number is K951917.

When did JOHNSON & JOHNSON EASY SLIDE DENTAL FLOSS receive FDA 510(k) clearance?

JOHNSON & JOHNSON EASY SLIDE DENTAL FLOSS received FDA 510(k) clearance on 1995-05-10, under 510(k) number K951917.

Who is the listed applicant for JOHNSON & JOHNSON EASY SLIDE DENTAL FLOSS?

The FDA 510(k) record lists Johnson & Johnson Consumer Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for JOHNSON & JOHNSON EASY SLIDE DENTAL FLOSS?

The FDA product code for JOHNSON & JOHNSON EASY SLIDE 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 Johnson & Johnson Consumer Products, Inc. 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.

View all 8 devices →

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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