AQUATINE EC ENDODONTIC CLEANSER
K-Number: K061689 · 2006-08-24
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Device Summary
Frequently Asked Questions
What is the AQUATINE EC ENDODONTIC CLEANSER?
AQUATINE EC ENDODONTIC CLEANSER is a medical device that received FDA 510(k) clearance on 2006-08-24. The listed applicant is Puricore, Inc.. The 510(k) number is K061689.
When did AQUATINE EC ENDODONTIC CLEANSER receive FDA 510(k) clearance?
AQUATINE EC ENDODONTIC CLEANSER received FDA 510(k) clearance on 2006-08-24, under 510(k) number K061689.
Who is the listed applicant for AQUATINE EC ENDODONTIC CLEANSER?
The FDA 510(k) record lists Puricore, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AQUATINE EC ENDODONTIC CLEANSER?
The FDA product code for AQUATINE EC ENDODONTIC CLEANSER is KJJ.
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 Puricore, 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: KJJ)
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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