Product code IPG— Physical Medicine

FDA has cleared 6 devices under product code IPG between 1976 and 2003, filed by 6 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

• 20031 clearance
• 19791 clearance
• 19782 clearances
• 19762 clearances

• Togard, Inc.1 clearance
• Richard'S Medical Equip., Inc.1 clearance
• Parke-Davis Co.1 clearance
• Ness-Neuromuscular Electrical Stimulation Systems1 clearance
• Cutler Biomedical1 clearance
• Ballert Orthopedic Corp.1 clearance

• K024279 — NESS CHILDREN SYSTEMNess-Neuromuscular Electrical Stimulation Systems·2003-02-05
• K790652 — TOGUARDTogard, Inc.·1979-04-04
• K781363 — CAST SHOECutler Biomedical·1978-08-14
• K780617 — EQUALIZERBallert Orthopedic Corp.·1978-04-18
• K760575 — ROCKER-SOLE CAST SANDALRichard'S Medical Equip., Inc.·1976-10-06
• K760578 — BALANCED CAST SOLEParke-Davis Co.·1976-09-27