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)

GOLD-PALLADIUM-SILVER BASED CAST/ALLOY

K-Number: K833736 · 1983-12-29

ApplicantJeneric Ind.
Decision Date1983-12-29
Product CodeEIS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

GOLD-PALLADIUM-SILVER BASED CAST/ALLOY is the device name listed in this FDA 510(k) record. The listed applicant is Jeneric Ind.. It received FDA 510(k) clearance on 1983-12-29 under 510(k) number K833736. The device is classified under product code EIS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GOLD-PALLADIUM-SILVER BASED CAST/ALLOY?

GOLD-PALLADIUM-SILVER BASED CAST/ALLOY is a medical device that received FDA 510(k) clearance on 1983-12-29. The listed applicant is Jeneric Ind.. The 510(k) number is K833736.

When did GOLD-PALLADIUM-SILVER BASED CAST/ALLOY receive FDA 510(k) clearance?

GOLD-PALLADIUM-SILVER BASED CAST/ALLOY received FDA 510(k) clearance on 1983-12-29, under 510(k) number K833736.

Who is the listed applicant for GOLD-PALLADIUM-SILVER BASED CAST/ALLOY?

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

What is the FDA product code for GOLD-PALLADIUM-SILVER BASED CAST/ALLOY?

The FDA product code for GOLD-PALLADIUM-SILVER BASED CAST/ALLOY is EIS.

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 Jeneric Ind. 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.

K862822REXILLIUM N. B. F.K862926SURGICAL VITEXK854878H40 BASE METAL ALLOYK844122RX CBGK844123RX CBYK840561RX ELAN

View all 25 devices →

Related Devices (Code: EIS)

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.

K992649ATD AUTOMATIC BRIDGE REMOVERJ. Morita USA, Inc.K951299EASY PNEUMATIC CROWN AND BRIDGE REMOVERDentco, Inc.K863500STAINLESS STEEL DEN. CROWN REMOVER & AMA./COMP.CARPacific Union Dental, Inc.K854795HAZELTON TEMPORARY CROWN AND BRIDGE REMOVERFran Hazelton Co.K842026H-TYPE BRIDGE REMOVERHiga Manufacturing , Ltd.K833287SATIN CAST ECONOCASTGenesis Industries, 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.

↑