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FDA 510(k)

DENTAL ROOT CANAL BACTERIALCIDAL LUBRICANT

K-Number: K921713 · 1993-11-04

ApplicantA and V Ent.
Decision Date1993-11-04
Product CodeKJJ
DecisionSubstantially Equivalent

Device Summary

DENTAL ROOT CANAL BACTERIALCIDAL LUBRICANT is the device name listed in this FDA 510(k) record. The listed applicant is A and V Ent.. It received FDA 510(k) clearance on 1993-11-04 under 510(k) number K921713. The device is classified under product code KJJ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DENTAL ROOT CANAL BACTERIALCIDAL LUBRICANT?

DENTAL ROOT CANAL BACTERIALCIDAL LUBRICANT is a medical device that received FDA 510(k) clearance on 1993-11-04. The listed applicant is A and V Ent.. The 510(k) number is K921713.

When did DENTAL ROOT CANAL BACTERIALCIDAL LUBRICANT receive FDA 510(k) clearance?

DENTAL ROOT CANAL BACTERIALCIDAL LUBRICANT received FDA 510(k) clearance on 1993-11-04, under 510(k) number K921713.

Who is the listed applicant for DENTAL ROOT CANAL BACTERIALCIDAL LUBRICANT?

The FDA 510(k) record lists A and V Ent. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DENTAL ROOT CANAL BACTERIALCIDAL LUBRICANT?

The FDA product code for DENTAL ROOT CANAL BACTERIALCIDAL LUBRICANT is KJJ.

Related Clinical Trials

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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.

K250279RC-SwiftPrepBelport Company, Inc., Gingi-PakK241354Sealer SolventInter-Med, Inc.K201785EPIEN Dental CleanserEpien Medical, Inc.K211813TritonInter-Med / Vista DentalK193357V-MixInter-Med/Vista Dental ProductsK193409Vista Rinse, Vista Rinse PlusInter-Med/Vista Dental Products

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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