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)

RIDGID VENA CAVA CANNULAE

K-Number: K802543 · 1981-01-16

ApplicantTexas Medical Products, Inc.
Decision Date1981-01-16
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RIDGID VENA CAVA CANNULAE is the device name listed in this FDA 510(k) record. The listed applicant is Texas Medical Products, Inc.. It received FDA 510(k) clearance on 1981-01-16 under 510(k) number K802543. The device is classified under product code DWF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RIDGID VENA CAVA CANNULAE?

RIDGID VENA CAVA CANNULAE is a medical device that received FDA 510(k) clearance on 1981-01-16. The listed applicant is Texas Medical Products, Inc.. The 510(k) number is K802543.

When did RIDGID VENA CAVA CANNULAE receive FDA 510(k) clearance?

RIDGID VENA CAVA CANNULAE received FDA 510(k) clearance on 1981-01-16, under 510(k) number K802543.

Who is the listed applicant for RIDGID VENA CAVA CANNULAE?

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

What is the FDA product code for RIDGID VENA CAVA CANNULAE?

The FDA product code for RIDGID VENA CAVA CANNULAE is DWF.

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 Texas 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.

K893417SURGIFRESH SUB-MICRON MASK NO. 901008-000K870932SURGIFRESH SURGICAL SMOKE REMOVALK851575DR. BRUNO LNAGE MINI PHOTOMETERK830634CARDIOTOMY FILTERK813587DISPOSABLE THORACIC CATHETERK810532DISPOSABLE STOPCOCK

View all 30 devices →

Related Devices (Code: DWF)

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.

K260195Elongated One-Piece Arterial (EOPA) 3D™ Arterial CannulaeMedtronic, Inc.K250937Venous Return CannulaeLivaNova USA, Inc.K260043Smart Reactors Camouflage Coated Extracorporeal Cardiopulmonary Tubing Set (SR180C)Smart ReactorsK253203Retrograde Coronary Sinus Perfusion CannulaeMedtronic, Inc.K253671Dual Stage Venous CannulaeSorin Group Italia S.R.L.K253998Clearview Intracoronary ShuntsMedtronic, 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.

↑