Product code ILZ— Physical Medicine

FDA has cleared 15 devices under product code ILZ between 1977 and 1992, filed by 11 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.

• 19921 clearance
• 19892 clearances
• 19852 clearances
• 19832 clearances
• 19823 clearances
• 19791 clearance
• 19783 clearances
• 19771 clearance

• Warm & Form, Orthopedic Materials3 clearances
• Biomet, Inc.3 clearances
• Will Ross Co.1 clearance
• Vibra-Trac Industries1 clearance
• Powlan Manufacturing Co.1 clearance
• Jerome Medical1 clearance
• Dyna-Med1 clearance
• Dr. K.G. Rude1 clearance
• D.C. Medical Device, Inc.1 clearance
• Chattanooga Group, Inc.1 clearance

• K921711 — FLEXION DISTRATION SUPPORTAltoona Medical Supply·1992-07-13
• K895382 — VIBRA-TRAC TRACTION TABLEVibra-Trac Industries·1989-10-16
• K884340 — AMX-110, AMX-II AND AMX-IIIDyna-Med·1989-01-24
• K852398 — VECTOR BAR SUSPENSION/TRACTION UNITPowlan Manufacturing Co.·1985-08-12
• K844490 — TRACTION ACCESSORIESJerome Medical·1985-02-21
• K831135 — SAUNDERS #7080 CERVICAL TRACTION SYSChattanooga Group, Inc.·1983-06-24
• K830245 — HEAD HALTERWarm & Form, Orthopedic Materials·1983-03-09
• K823659 — PELVIC TRACTION BELTWarm & Form, Orthopedic Materials·1982-12-30
• K823166 — PELVIC TRACTION BELTWarm & Form, Orthopedic Materials·1982-11-10
• K820663 — BOGER AUTO-TRACTION DEVICED.C. Medical Device, Inc.·1982-05-03
• K791808 — CERVI-TRACDr. K.G. Rude·1979-10-01
• K780227 — BANDAGE SPREADER BLOCKBiomet, Inc.·1978-03-15
• K780234 — TRACTION BELT, PELVICBiomet, Inc.·1978-02-23
• K780226 — SPREADER BARSBiomet, Inc.·1978-02-17
• K770607 — TRACTION HARNESSWill Ross Co.·1977-04-08