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)

DUAL LUMEN 5 FR PERIP CENT VEN CATH W/GROSHONG VAL

K-Number: K904558 · 1991-02-11

ApplicantDavol, Inc.
Decision Date1991-02-11
Product CodeFOZ
Advisory CommitteeHO
DecisionUnknown

Device Summary

DUAL LUMEN 5 FR PERIP CENT VEN CATH W/GROSHONG VAL is the device name listed in this FDA 510(k) record. The listed applicant is Davol, Inc.. It received FDA 510(k) clearance on 1991-02-11 under 510(k) number K904558. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the DUAL LUMEN 5 FR PERIP CENT VEN CATH W/GROSHONG VAL?

DUAL LUMEN 5 FR PERIP CENT VEN CATH W/GROSHONG VAL is a medical device that received FDA 510(k) clearance on 1991-02-11. The listed applicant is Davol, Inc.. The 510(k) number is K904558.

When did DUAL LUMEN 5 FR PERIP CENT VEN CATH W/GROSHONG VAL receive FDA 510(k) clearance?

DUAL LUMEN 5 FR PERIP CENT VEN CATH W/GROSHONG VAL received FDA 510(k) clearance on 1991-02-11, under 510(k) number K904558.

Who is the listed applicant for DUAL LUMEN 5 FR PERIP CENT VEN CATH W/GROSHONG VAL?

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

What is the FDA product code for DUAL LUMEN 5 FR PERIP CENT VEN CATH W/GROSHONG VAL?

The FDA product code for DUAL LUMEN 5 FR PERIP CENT VEN CATH W/GROSHONG VAL is FOZ.

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 Davol, 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.

K251557Bard® Mesh; Bard® Mesh Pre-ShapedK250098Bard Soft Mesh; Bard Soft Mesh Pre-ShapedK031213AQUASENS FLUID MONITORING SYSTEMK030307DAVOL ARTHROVENT OUTFLOW TUBINGK003323COMPOSIX KUGEL MESH, MODEL 0010201,0010202,0010203,0010204,0010205K003790DAVOL X-STREAM LAPAROSCOPIC IRRIGATION SYSTEM, MODELS 5551000, 5552000, 5552001, 552002, 5552003, 5552004, 5552005

View all 50 devices →

Related Devices (Code: FOZ)

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.

K260432Ruby Intravascular CatheterVenocare, Inc.K260165Unimpregnated Central Venous CatheterSpectrum VascularK261041ClearSafe Closed SystemMedSource Labs, LLCK260539MedSource QuickSafe™ Safety IV Catheter; MedSource PurSafe™ Safety IV CatheterMedSource Labs, LLCK253235Introcan Safety® Deep Access XL IV CatheterB.Braun Medical, Inc.K252137BD Insyte™ IV CatheterBecton Dickinson Infusion Therapy Systems, 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.

↑