Product code IKD— Physical Medicine

FDA has cleared 6 devices under product code IKD between 1980 and 2007, filed by 6 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

• 20071 clearance
• 19991 clearance
• 19931 clearance
• 19871 clearance
• 19841 clearance
• 19801 clearance

• Therapy Equipment, Inc.1 clearance
• R2 Corp.1 clearance
• Quinton, Inc.1 clearance
• Physiometrix, Inc.1 clearance
• Oscor, Inc.1 clearance
• Chemfet Corp.1 clearance

• K070926 — ELECTRODE/EXTENSION CABLES, MODELS ATAROscor, Inc.·2007-06-07
• K992372 — THE LEADAWAYTherapy Equipment, Inc.·1999-10-13
• K935260 — PHYSIOMETRIX CABLE ADAPTER MODIFICATIONPhysiometrix, Inc.·1993-12-23
• K873361 — LIFE-SPAN CABLEChemfet Corp.·1987-11-09
• K834583 — CLEAR LEADS-RADIOTRANSPARENT WIRESQuinton, Inc.·1984-01-30
• K800934 — R2 ESU CABLE-ADAPTER MODELS 160,161R2 Corp.·1980-05-20