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FDA 510(k)

OXY-GLIDE ROOT CANAL CLEANSER & LUB.

K-Number: K992919 · 1999-11-19

ApplicantSuper Glide, Inc.
Decision Date1999-11-19
Product CodeKJJ
DecisionSubstantially Equivalent

Device Summary

OXY-GLIDE ROOT CANAL CLEANSER & LUB. is the device name listed in this FDA 510(k) record. The listed applicant is Super Glide, Inc.. It received FDA 510(k) clearance on 1999-11-19 under 510(k) number K992919. The device is classified under product code KJJ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OXY-GLIDE ROOT CANAL CLEANSER & LUB.?

OXY-GLIDE ROOT CANAL CLEANSER & LUB. is a medical device that received FDA 510(k) clearance on 1999-11-19. The listed applicant is Super Glide, Inc.. The 510(k) number is K992919.

When did OXY-GLIDE ROOT CANAL CLEANSER & LUB. receive FDA 510(k) clearance?

OXY-GLIDE ROOT CANAL CLEANSER & LUB. received FDA 510(k) clearance on 1999-11-19, under 510(k) number K992919.

Who is the listed applicant for OXY-GLIDE ROOT CANAL CLEANSER & LUB.?

The FDA 510(k) record lists Super Glide, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OXY-GLIDE ROOT CANAL CLEANSER & LUB.?

The FDA product code for OXY-GLIDE ROOT CANAL CLEANSER & LUB. 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.

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Other records listing Super Glide, 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.

K003422EDTA ROOT CANAL CLEANSER

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

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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