JOHNSON & JOHNSON EASY SLIDE DENTAL FLOSS
K-Number: K951917 · 1995-05-10
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Device Summary
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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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