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FDA 510(k)

VERSADOWEL POST SYSTEM

K-Number: K940680 · 1994-03-15

ApplicantDental Power, Inc.
Decision Date1994-03-15
Product CodeELR
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VERSADOWEL POST SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Dental Power, Inc.. It received FDA 510(k) clearance on 1994-03-15 under 510(k) number K940680. The device is classified under product code ELR. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VERSADOWEL POST SYSTEM?

VERSADOWEL POST SYSTEM is a medical device that received FDA 510(k) clearance on 1994-03-15. The listed applicant is Dental Power, Inc.. The 510(k) number is K940680.

When did VERSADOWEL POST SYSTEM receive FDA 510(k) clearance?

VERSADOWEL POST SYSTEM received FDA 510(k) clearance on 1994-03-15, under 510(k) number K940680.

Who is the listed applicant for VERSADOWEL POST SYSTEM?

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

What is the FDA product code for VERSADOWEL POST SYSTEM?

The FDA product code for VERSADOWEL POST SYSTEM is ELR.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Dental Power, 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.

K004031NT SWIFT; TI\TEC; GATES GLIDDEN DRILLS; DENTAL POWER ENDODONTIC HAND FILES

Related Devices (Code: ELR)

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.

K060075FIBER-METAL POSTForemost Dental, LLCK042848FRC POSTEC PLUSIvoclar Vivadent, Inc.K030820EVERSTICK POSTStick Tech , Ltd.K020431FIBIOCOREEst. AnthogyrK012496CARBON POSTJ. Morita USA, Inc.K013802FRC POSTECIvoclar Vivadent, Inc.

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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