COLGATE DENTAL FLOSS
K-Number: K883335 · 1988-08-26
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Device Summary
Frequently Asked Questions
What is the COLGATE DENTAL FLOSS?
COLGATE DENTAL FLOSS is a medical device that received FDA 510(k) clearance on 1988-08-26. The listed applicant is Colgate-Palmolive Co.. The 510(k) number is K883335.
When did COLGATE DENTAL FLOSS receive FDA 510(k) clearance?
COLGATE DENTAL FLOSS received FDA 510(k) clearance on 1988-08-26, under 510(k) number K883335.
Who is the listed applicant for COLGATE DENTAL FLOSS?
The FDA 510(k) record lists Colgate-Palmolive Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COLGATE DENTAL FLOSS?
The FDA product code for COLGATE 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 Colgate-Palmolive Co. 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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