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FDA 510(k)

RSI FEMORAL GUIDING CATHETER

K-Number: K902943 · 1990-10-03

ApplicantRetroperfusion Systems, Inc.
Decision Date1990-10-03
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RSI FEMORAL GUIDING CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Retroperfusion Systems, Inc.. It received FDA 510(k) clearance on 1990-10-03 under 510(k) number K902943. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RSI FEMORAL GUIDING CATHETER?

RSI FEMORAL GUIDING CATHETER is a medical device that received FDA 510(k) clearance on 1990-10-03. The listed applicant is Retroperfusion Systems, Inc.. The 510(k) number is K902943.

When did RSI FEMORAL GUIDING CATHETER receive FDA 510(k) clearance?

RSI FEMORAL GUIDING CATHETER received FDA 510(k) clearance on 1990-10-03, under 510(k) number K902943.

Who is the listed applicant for RSI FEMORAL GUIDING CATHETER?

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

What is the FDA product code for RSI FEMORAL GUIDING CATHETER?

The FDA product code for RSI FEMORAL GUIDING CATHETER is DQO.

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 Retroperfusion Systems, 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.

K865074CORDAY CORONARY SINUS INFUSION CATHETER

Related Devices (Code: DQO)

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.

K261455Arterial Pressure Monitoring Set/TraySpectrum VascularK252702Bioptimal Pulmonary Artery Monitoring Catheter (TD2502NF, TD2502NGF, TD2502NDF, TD2502NCF, TD2502NCGF, TD2502NDGF, TD2502NDCF, TD2502NDCGF, TD2502NXCF, TD2502NDXF, TD2502NXCGF, TD2502NDXGF, TD2502NDXCF, TD2502NDXCGF, TD2502-110NF, TD2502-110NGF, TD2502-110NDF, TD2502-110NCF, TD2502-110NDGF, TD2502-110NDCF, TD2502-110NCGF, TD2502-110NDCGF, TD2502-110NXF, TD2502-110NXGF, TD2502-110NDXF, TD2502-110NXCF, TD2502-110NDXGF, TD2502-110NDXCF ,TD2502-110NXCGF, TD2502-110NDXCGF, TD2602NF, TD2602NBioptimal International Pte. , Ltd.K254278Arterial Pressure Monitoring Set/TraySpectrum VascularK250751DualView CatheterTerumo CorporationK242966Gentuity® HF-OCT Imaging System with Vis-Rx Prime® Micro-Imaging CatheterGentuity, LLCK242420pNOVUS 21 MicrocatheterPhenox, Ltd.

Official Source

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