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)

VASCULAR GRAFT/BIFURCATED/FEP-RINGED

K-Number: K830806 · 1983-08-13

ApplicantW. L. Gore & Associates, Inc.
Decision Date1983-08-13
Product CodeDXZ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VASCULAR GRAFT/BIFURCATED/FEP-RINGED is the device name listed in this FDA 510(k) record. The listed applicant is W. L. Gore & Associates, Inc.. It received FDA 510(k) clearance on 1983-08-13 under 510(k) number K830806. The device is classified under product code DXZ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VASCULAR GRAFT/BIFURCATED/FEP-RINGED?

VASCULAR GRAFT/BIFURCATED/FEP-RINGED is a medical device that received FDA 510(k) clearance on 1983-08-13. The listed applicant is W. L. Gore & Associates, Inc.. The 510(k) number is K830806.

When did VASCULAR GRAFT/BIFURCATED/FEP-RINGED receive FDA 510(k) clearance?

VASCULAR GRAFT/BIFURCATED/FEP-RINGED received FDA 510(k) clearance on 1983-08-13, under 510(k) number K830806.

Who is the listed applicant for VASCULAR GRAFT/BIFURCATED/FEP-RINGED?

The FDA 510(k) record lists W. L. Gore & Associates, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VASCULAR GRAFT/BIFURCATED/FEP-RINGED?

The FDA product code for VASCULAR GRAFT/BIFURCATED/FEP-RINGED is DXZ.

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 W. L. Gore & Associates, 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.

K250410GORE® Tri-Lobe Balloon CatheterK240083GORE® PROPATEN® Vascular GraftK232312GORE® PROPATEN® Vascular GraftK233551GORE® ACUSEAL Vascular GraftK231505GORE® ACUSEAL Vascular GraftK222919GORE® ENFORM Biomaterial

View all 163 devices →

Related Devices (Code: DXZ)

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.

K240775PeriBeam® Pericardial MembraneTamabioK200955Vascutek Gelseal Patch, Vascutek Gelsoft Patch, Vascutek Thin Wall Carotid PatchVascutek, Ltd.K162506PhotoFix Decellularized Bovine PericardiumCryolife, Inc.K162579VascuCelAdmedus Regen Pty, Ltd.K152127CorMatrix TykeCormatrix Cardiovascular, Inc.K122306SYNOVIS COLLAGEN MATRIX (TBD)Synovis Surgical Innovations

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.

↑