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)

CLASSIC RESTING SILVER-SILVERCHLORIDE ELECTRODE

K-Number: K862953 · 1986-08-25

ApplicantClassic Medical Products, Inc.
Decision Date1986-08-25
Product CodeDRY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CLASSIC RESTING SILVER-SILVERCHLORIDE ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Classic Medical Products, Inc.. It received FDA 510(k) clearance on 1986-08-25 under 510(k) number K862953. The device is classified under product code DRY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLASSIC RESTING SILVER-SILVERCHLORIDE ELECTRODE?

CLASSIC RESTING SILVER-SILVERCHLORIDE ELECTRODE is a medical device that received FDA 510(k) clearance on 1986-08-25. The listed applicant is Classic Medical Products, Inc.. The 510(k) number is K862953.

When did CLASSIC RESTING SILVER-SILVERCHLORIDE ELECTRODE receive FDA 510(k) clearance?

CLASSIC RESTING SILVER-SILVERCHLORIDE ELECTRODE received FDA 510(k) clearance on 1986-08-25, under 510(k) number K862953.

Who is the listed applicant for CLASSIC RESTING SILVER-SILVERCHLORIDE ELECTRODE?

The FDA 510(k) record lists Classic Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CLASSIC RESTING SILVER-SILVERCHLORIDE ELECTRODE?

The FDA product code for CLASSIC RESTING SILVER-SILVERCHLORIDE ELECTRODE is DRY.

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 Classic Medical Products, 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.

K900519CLASSIC ECG/STIMULATING NO. 1700 SERIES

Related Devices (Code: DRY)

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.

K234065CDI OneView Monitoring SystemTerumo Cardiovascular Systems CorporationK202154B-CaptaLivanova Deutschland, GmbHK202557Quantum Workstation 12 EliteSpectrum Medical , Ltd.K182110CDI Blood Parameter Monitoring System 550Terumo Cardiovascular Systems CorporationK181923Quantum Workstation 12.1Spectrum Medical , Ltd.K173591Quantum Diagnostic Module, Quantum Diagnostic Module - No GasSpectrum Medical , Ltd.

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.

↑