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)

ELECTRODE/EXTENSION CABLES, MODELS ATAR

K-Number: K070926 · 2007-06-07

ApplicantOscor, Inc.
Decision Date2007-06-07
Product CodeIKD
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ELECTRODE/EXTENSION CABLES, MODELS ATAR is the device name listed in this FDA 510(k) record. The listed applicant is Oscor, Inc.. It received FDA 510(k) clearance on 2007-06-07 under 510(k) number K070926. The device is classified under product code IKD. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTRODE/EXTENSION CABLES, MODELS ATAR?

ELECTRODE/EXTENSION CABLES, MODELS ATAR is a medical device that received FDA 510(k) clearance on 2007-06-07. The listed applicant is Oscor, Inc.. The 510(k) number is K070926.

When did ELECTRODE/EXTENSION CABLES, MODELS ATAR receive FDA 510(k) clearance?

ELECTRODE/EXTENSION CABLES, MODELS ATAR received FDA 510(k) clearance on 2007-06-07, under 510(k) number K070926.

Who is the listed applicant for ELECTRODE/EXTENSION CABLES, MODELS ATAR?

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

What is the FDA product code for ELECTRODE/EXTENSION CABLES, MODELS ATAR?

The FDA product code for ELECTRODE/EXTENSION CABLES, MODELS ATAR is IKD.

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 Oscor, 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.

K210627Breezeway IIK130104GUIDEWIRE, PURSUER SERIESK122958DELIVERY SHEATH, MODEL ADELANTE BREEZEWAYK122960STEERABLE GUIDING SHEATH, MODEL ADELANTE DESTINOK122084INTRODUCER SET, MODEL ADELANTE-S SERIESK120459STEERABLE GUIDING SHEATH, MODEL ADELANTE DESTINO

View all 43 devices →

Related Devices (Code: IKD)

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.

K992372THE LEADAWAYTherapy Equipment, Inc.K935260PHYSIOMETRIX CABLE ADAPTER MODIFICATIONPhysiometrix, Inc.K873361LIFE-SPAN CABLEChemfet Corp.K834583CLEAR LEADS-RADIOTRANSPARENT WIRESQuinton, Inc.K800934R2 ESU CABLE-ADAPTER MODELS 160,161R2 Corp.

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.

↑