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)

CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATH SET

K-Number: K914936 · 1992-04-23

ApplicantAkcess Medical Products, Inc.
Decision Date1992-04-23
Product CodeLFK
Advisory CommitteeGU
DecisionUnknown

Device Summary

CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATH SET is the device name listed in this FDA 510(k) record. The listed applicant is Akcess Medical Products, Inc.. It received FDA 510(k) clearance on 1992-04-23 under 510(k) number K914936. The device is classified under product code LFK. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATH SET?

CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATH SET is a medical device that received FDA 510(k) clearance on 1992-04-23. The listed applicant is Akcess Medical Products, Inc.. The 510(k) number is K914936.

When did CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATH SET receive FDA 510(k) clearance?

CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATH SET received FDA 510(k) clearance on 1992-04-23, under 510(k) number K914936.

Who is the listed applicant for CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATH SET?

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

What is the FDA product code for CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATH SET?

The FDA product code for CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATH SET is LFK.

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 Akcess 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.

K926374SILICONE CATHETER REPAIR KITSK925819AKCESS0CATH KITK925818AKCESS-CATHK930630RIGHT ATRIAL CATHETERK931120COAXIAL ACUTE CATHETERK920634SPLITTABLE SHEATH INTRODUCER SET

View all 36 devices →

Related Devices (Code: LFK)

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.

K971897CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATHETER 10 FR (CAVH)Medron, Inc.K915215CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATH. KITSAkcess Medical Products, Inc.K891763FC-100 FEMORAL CATHETERAkcess Medical Products, Inc.K891764FC-101 FEMORAL CATHETER GUIDE WIREAkcess Medical Products, Inc.K890717MODIFICATION HEMOFILTRATION CATHETER HF-100Vas-Cath, Inc.K880775CONTINUOUS ARTERIAL/VENOUS HEMOFILTRATION TRAYMedsurg Industries, 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.

↑