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)

NEYDIUM NPFLUX (FOR SOLDERING)

K-Number: K770159 · 1977-01-31

ApplicantDeringer-Ney, Inc.
Decision Date1977-01-31
Product Code
DecisionSubstantially Equivalent

Device Summary

NEYDIUM NPFLUX (FOR SOLDERING) is the device name listed in this FDA 510(k) record. The listed applicant is Deringer-Ney, Inc.. It received FDA 510(k) clearance on 1977-01-31 under 510(k) number K770159. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEYDIUM NPFLUX (FOR SOLDERING)?

NEYDIUM NPFLUX (FOR SOLDERING) is a medical device that received FDA 510(k) clearance on 1977-01-31. The listed applicant is Deringer-Ney, Inc.. The 510(k) number is K770159.

When did NEYDIUM NPFLUX (FOR SOLDERING) receive FDA 510(k) clearance?

NEYDIUM NPFLUX (FOR SOLDERING) received FDA 510(k) clearance on 1977-01-31, under 510(k) number K770159.

Who is the listed applicant for NEYDIUM NPFLUX (FOR SOLDERING)?

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

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 Deringer-Ney, 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.

K933178GDC 3509K930482DENTAL CASTING ALLOY, MODIFICATION - PF-3K930481DENTAL CASTING ALLOY MODIFICATION-PF-4K925273GDC 3445K920922GDC 3367K920060DENTAL SOLDER ALLOY

View all 46 devices →

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.

↑