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FDA 510(k)

ENDOSOLV E

K-Number: K780003 · 1978-01-20

ApplicantSeptodont, Inc.
Decision Date1978-01-20
Product CodeKJJ
DecisionSubstantially Equivalent

Device Summary

ENDOSOLV E is the device name listed in this FDA 510(k) record. The listed applicant is Septodont, Inc.. It received FDA 510(k) clearance on 1978-01-20 under 510(k) number K780003. The device is classified under product code KJJ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOSOLV E?

ENDOSOLV E is a medical device that received FDA 510(k) clearance on 1978-01-20. The listed applicant is Septodont, Inc.. The 510(k) number is K780003.

When did ENDOSOLV E receive FDA 510(k) clearance?

ENDOSOLV E received FDA 510(k) clearance on 1978-01-20, under 510(k) number K780003.

Who is the listed applicant for ENDOSOLV E?

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

What is the FDA product code for ENDOSOLV E?

The FDA product code for ENDOSOLV E is KJJ.

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Other records listing Septodont, 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.

K771114NEUTROCIMK761354CIMPAT (PINK AND WHITE)K761355SELFASTK760798FLUOCAL GEL MINTK760799FLUOCAL GEL ORANGEK761024RACESTYPTINE RINGS

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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

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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