FDA 510(k)

RADTECH VASCULAR STENT

K-Number: K860763 · 1986-03-28

Decision Date1986-03-28

Product Code

DecisionSubstantially Equivalent

Device Summary

RADTECH VASCULAR STENT is the device name listed in this FDA 510(k) record. The listed applicant is Radtech, Inc.. It received FDA 510(k) clearance on 1986-03-28 under 510(k) number K860763. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RADTECH VASCULAR STENT?

RADTECH VASCULAR STENT is a medical device that received FDA 510(k) clearance on 1986-03-28. The listed applicant is Radtech, Inc.. The 510(k) number is K860763.

When did RADTECH VASCULAR STENT receive FDA 510(k) clearance?

RADTECH VASCULAR STENT received FDA 510(k) clearance on 1986-03-28, under 510(k) number K860763.

Who is the listed applicant for RADTECH VASCULAR STENT?

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

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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Radtech, Inc. as applicant

K861453STAGNONE SWIVEL-JOINT NEEDLE

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.