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)

DISPERSED PHASE ALLOY

K-Number: K820617 · 1982-03-25

ApplicantGoldsmith & Revere, Inc.
Decision Date1982-03-25
Product CodeEJJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DISPERSED PHASE ALLOY is the device name listed in this FDA 510(k) record. The listed applicant is Goldsmith & Revere, Inc.. It received FDA 510(k) clearance on 1982-03-25 under 510(k) number K820617. The device is classified under product code EJJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPERSED PHASE ALLOY?

DISPERSED PHASE ALLOY is a medical device that received FDA 510(k) clearance on 1982-03-25. The listed applicant is Goldsmith & Revere, Inc.. The 510(k) number is K820617.

When did DISPERSED PHASE ALLOY receive FDA 510(k) clearance?

DISPERSED PHASE ALLOY received FDA 510(k) clearance on 1982-03-25, under 510(k) number K820617.

Who is the listed applicant for DISPERSED PHASE ALLOY?

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

What is the FDA product code for DISPERSED PHASE ALLOY?

The FDA product code for DISPERSED PHASE ALLOY is EJJ.

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 Goldsmith & Revere, 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.

K951865ULTRA SPHERICAL AMALGAM ALLOYK933309PRINCEK821222GOLDSMITH & REVERE TENARY ALLOY

Related Devices (Code: EJJ)

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.

K053114SILVERFILDunia Perwira Manufacturing Sdn. Bhd.K051010SECURALLOY, SEPTALLOY NG 50 AND SEPTALLOY NG 70SeptodontK033434BESTALOYWe Dong Myung Dental Industrial Co., Ltd.K032152BENCO ADMIXSouthern Dental Industries, Inc.K031658BENCO SPHERICALSouthern Dental Industries, Inc.K020452HIGH SILVER CONVENTIONALAb Ardent

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.

↑