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FDA 510(k)

EPIC CANNULA

K-Number: K792578 · 1980-01-04

ApplicantDental Development Services, Inc.
Decision Date1980-01-04
Product CodeEIC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

EPIC CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Dental Development Services, Inc.. It received FDA 510(k) clearance on 1980-01-04 under 510(k) number K792578. 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 EPIC CANNULA?

EPIC CANNULA is a medical device that received FDA 510(k) clearance on 1980-01-04. The listed applicant is Dental Development Services, Inc.. The 510(k) number is K792578.

When did EPIC CANNULA receive FDA 510(k) clearance?

EPIC CANNULA received FDA 510(k) clearance on 1980-01-04, under 510(k) number K792578.

Who is the listed applicant for EPIC CANNULA?

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

What is the FDA product code for EPIC CANNULA?

The FDA product code for EPIC CANNULA 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 Dental Development Services, 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.

K792577ENDOVAGE SYRINGE

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.

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