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FDA 510(k)

CLEANSER ROOT CANAL

K-Number: K130180 · 2013-10-03

ApplicantCerkamed Wojciech Pawlowski
Decision Date2013-10-03
Product CodeKJJ
DecisionSubstantially Equivalent

Device Summary

CLEANSER ROOT CANAL is the device name listed in this FDA 510(k) record. The listed applicant is Cerkamed Wojciech Pawlowski. It received FDA 510(k) clearance on 2013-10-03 under 510(k) number K130180. The device is classified under product code KJJ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLEANSER ROOT CANAL?

CLEANSER ROOT CANAL is a medical device that received FDA 510(k) clearance on 2013-10-03. The listed applicant is Cerkamed Wojciech Pawlowski. The 510(k) number is K130180.

When did CLEANSER ROOT CANAL receive FDA 510(k) clearance?

CLEANSER ROOT CANAL received FDA 510(k) clearance on 2013-10-03, under 510(k) number K130180.

Who is the listed applicant for CLEANSER ROOT CANAL?

The FDA 510(k) record lists Cerkamed Wojciech Pawlowski as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CLEANSER ROOT CANAL?

The FDA product code for CLEANSER ROOT CANAL is KJJ.

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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.

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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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