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)

STRESS/EMERGENCY EELCTRODE

K-Number: K790883 · 1979-07-24

ApplicantHayes Products, Inc.
Decision Date1979-07-24
Product Code
DecisionSubstantially Equivalent

Device Summary

STRESS/EMERGENCY EELCTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Hayes Products, Inc.. It received FDA 510(k) clearance on 1979-07-24 under 510(k) number K790883. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRESS/EMERGENCY EELCTRODE?

STRESS/EMERGENCY EELCTRODE is a medical device that received FDA 510(k) clearance on 1979-07-24. The listed applicant is Hayes Products, Inc.. The 510(k) number is K790883.

When did STRESS/EMERGENCY EELCTRODE receive FDA 510(k) clearance?

STRESS/EMERGENCY EELCTRODE received FDA 510(k) clearance on 1979-07-24, under 510(k) number K790883.

Who is the listed applicant for STRESS/EMERGENCY EELCTRODE?

The FDA 510(k) record lists Hayes Products, 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 Hayes 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.

K791139PREGELLED DISPOSABLE ECG ELECTRODESK791140PREGELLED DISPOSABLE EELCTRO. SERIES 600K781940EKG ELECTRODES, DISPOSABLEK771447PREGELLED DISP. EKG MONITORING ELECT-

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.

↑