Ideas Occluder

FDA 510(k) K935964 · Ideas For Medicine, Inc.

Substantially Equivalent

510(k) numberK935964

Submission

Device name
Ideas Occluder
Applicant
Ideas For Medicine, Inc.
Clearwater, FL, US
Received
December 13, 1993
Decision date
January 4, 1995
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
DXC – Clamp, Vascular
Device class
Class II (moderate risk)
Regulation
21 CFR 870.4450
Specialty
Cardiovascular

Other 510(k)s with product code DXC

510(k)DeviceApplicantDecision
K262086PreludeSYNC™ Radial Compression DeviceDXC · Special Merit Medical Systems, Inc.07/22/2026SE
K260105Fogarty Spring Clips, Handleless Clamps, and Clamp InsertsDXC · Traditional Edwards Lifesciences06/05/2026SE
K252772Arc Adjustable Radial Cuff Compression DeviceDXC · Traditional Tz Medical, Inc.05/22/2026SE
K254060Life Saving TourniquetDXC · Traditional TW Medical04/03/2026SE
K243627Laryngoscope Junctional-Arterial Restriction Clamp (L-ARC); Arterial Restriction Clamp…DXC · Traditional Arc Trauma, LLC12/31/2025SE
K253070Namic Radial Arm Band, 23 cm (DYNJRADBAND); Namic Radial Arm Band, 26 cm (DYNJRADBANDL)DXC · Traditional Medline Industries, LP11/20/2025SE
K232577Radial Compression DeviceDXC · Traditional Ningbo Dizegens Medical Science Co.,Ltd01/18/2024SE
K230281PicoclampDXC · Traditional Kono Seisakusho Co., Ltd.10/23/2023SE
K221661Abdominal Aortic and Junctional Tourniquet - Stabilized (AAJT-S)DXC · Traditional Compression Works, Inc.03/03/2023SE
K230248ViolaDXC · Special Vascular Graft Solutions, Ltd.02/28/2023SE

More from Vascular Graft Solutions, Ltd.

510(k)DeviceDecision
K961883Versa-Cath Arterial CatheterDXE · Traditional 01/13/1997SE
K962751Ideas' Dual PortLJT · Traditional 09/30/1996SE
K961716Vaso-Safe Arterial Embolectomy CatheteDXE · Traditional 09/19/1996SE
K960715Pruitt-Inahara Carotid Shunt 400-40-8F/INAHARA-PRUITT Carotid Shunt 500-50-8FMJN · Traditional 09/09/1996SE
K960422Pruitt Safety Occlusion CatheterMJN · Traditional 08/07/1996SE
K954713Dural-Lumen Intra Vascular Balloon Catheter (Modification)FGE · Traditional 07/24/1996SE
K935023Godat Uterine Manipulator InjectorLKF · Traditional 01/04/1995SE
K880231Modified Pruitt Irrigation & Occlusion CatheterDQT · Traditional 05/25/1988SE
K872090The Robicsek - Pruitt Aortic Balloon Occlusion KitDQT · Traditional 10/30/1987SE
K872485Change of Catheter Body Material (Radio-Opaque Ny)DXE · Traditional 08/12/1987SE

Questions and answers

When was Ideas Occluder cleared by the FDA?

Ideas Occluder (K935964) received a 510(k) decision of Substantially Equivalent on January 4, 1995, 387 days after the submission was received.

What is the product code of K935964?

The FDA product code is DXC – Clamp, Vascular, a Class II (moderate risk) device regulated under 21 CFR 870.4450.