Product code IQF— Physical Medicine

FDA has cleared 7 devices under product code IQF between 1978 and 1983, filed by 5 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.

• 19831 clearance
• 19813 clearances
• 19791 clearance
• 19782 clearances

• Orthomedics3 clearances
• Zee Medical Products Co., Inc.1 clearance
• Medi-Ked, Inc.1 clearance
• Marullo, Baldwin, Frieden, Gatewood,1 clearance
• Hospital Products Co.1 clearance

• K832741 — JASON CERVICAL ORTHOSISOrthomedics·1983-09-20
• K812342 — ZEE EXTRICATION DEVICEZee Medical Products Co., Inc.·1981-09-21
• K811297 — CERVICAL SUPPORTOrthomedics·1981-05-27
• K810555 — SCOLIOSIS ORTHOTIC SYSTEMOrthomedics·1981-03-13
• K791350 — POPE AMBULATORY HALO VESTHospital Products Co.·1979-08-03
• K781761 — KENDRICK EXTRICATION DEVICEMedi-Ked, Inc.·1978-10-27
• K780489 — SPINE BOARDMarullo, Baldwin, Frieden, Gatewood,·1978-04-12