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)

RELIANCE 1379

K-Number: K853359 · 1985-09-24

ApplicantDentsply Intl.
Decision Date1985-09-24
Product CodeHRJ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

RELIANCE 1379 is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 1985-09-24 under 510(k) number K853359. The device is classified under product code HRJ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RELIANCE 1379?

RELIANCE 1379 is a medical device that received FDA 510(k) clearance on 1985-09-24. The listed applicant is Dentsply Intl.. The 510(k) number is K853359.

When did RELIANCE 1379 receive FDA 510(k) clearance?

RELIANCE 1379 received FDA 510(k) clearance on 1985-09-24, under 510(k) number K853359.

Who is the listed applicant for RELIANCE 1379?

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

What is the FDA product code for RELIANCE 1379?

The FDA product code for RELIANCE 1379 is HRJ.

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 Dentsply Intl. 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.

K123615IRIS - HIGH STRENGTH GLASS CERAMICK072730FRIADENT CERCON AND ANKYLOS CERCON BALANCE ABUTMENTSK070538XP BOND DUAL CURE UNIVERSAL TOTAL ETCH ADHESIVEK070019CARRARA VOLUMIAK061427PRE-IMPRESSION CONDITIONING SOLUTIONK052334CAVITRON RF ULTRASONIC SCALER SYSTEM WITH STERIMATE HANDPIECE, MODEL G-131

View all 279 devices →

Related Devices (Code: HRJ)

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.

K930447MARCO H AND TS-1 INSTRUMENT TABLESMarco Ophthalmic, Inc.K922242910T MONTORIZED INSTRUMENT TABLER.H. Burton Co.K912134TBD, LENS MEASURING DEVICEAlcon LaboratoriesK853744TECHNA VISION, INC.ELECTRIC TABLETechna VisionK841760WOODLYN CLASSIC INSTRUMENT STANDWoodlyn, Inc.K833820MACHEMER/TANO ROTATINGOptical Micro Systems, 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.

↑