Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CENTRIX MKIV ENDODONTIC DELIVERY

K-Number: K792461 · 1979-12-19

ApplicantCentrix, Inc.
Decision Date1979-12-19
Product CodeEIC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CENTRIX MKIV ENDODONTIC DELIVERY is the device name listed in this FDA 510(k) record. The listed applicant is Centrix, Inc.. It received FDA 510(k) clearance on 1979-12-19 under 510(k) number K792461. The device is classified under product code EIC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CENTRIX MKIV ENDODONTIC DELIVERY?

CENTRIX MKIV ENDODONTIC DELIVERY is a medical device that received FDA 510(k) clearance on 1979-12-19. The listed applicant is Centrix, Inc.. The 510(k) number is K792461.

When did CENTRIX MKIV ENDODONTIC DELIVERY receive FDA 510(k) clearance?

CENTRIX MKIV ENDODONTIC DELIVERY received FDA 510(k) clearance on 1979-12-19, under 510(k) number K792461.

Who is the listed applicant for CENTRIX MKIV ENDODONTIC DELIVERY?

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

What is the FDA product code for CENTRIX MKIV ENDODONTIC DELIVERY?

The FDA product code for CENTRIX MKIV ENDODONTIC DELIVERY is EIC.

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 Centrix, 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.

K250714FluoroDose VarnishK222459Centrix FluoroSilver Silver Diamine Fluoride 38%K152826NoCordK120176SENZZZZZ AWAYK111348RE / STASIS (TM) GINGIVAL RETRACTION PASTEK092384LIQUICORD

View all 46 devices →

Related Devices (Code: EIC)

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.

K972234RCT GEL ROOT CANAL THERAPY GELDentsply Intl.K864307MAX-I-PROBE PERIDONTAL/ENDODONTIC PROBE(TM) (MODI)Smith & Nephew, Inc.K861846HYDRON ROOT CANAL FILLING & MARK IV STARTER KITSolar Dental Co., Inc.K851944MAX-I-PROBE HANDPIECESolo Pak LaboratoriesK840237MAX-I-PROBE PERIODONTAL ENDODONTIC PROBSmith & Nephew, Mpl DivisionK811889R & S SERIES FITTING TOOLSSuncoast Dental Corp.

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.

↑