Boger Auto-Traction Device

FDA 510(k) K820663 · D.C. Medical Device, Inc.

Substantially Equivalent

510(k) numberK820663

Submission

Device name
Boger Auto-Traction Device
Applicant
D.C. Medical Device, Inc.
Mchenry, IL, US
Received
March 10, 1982
Decision date
May 3, 1982
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
ILZ – Accessories, Traction
Device class
Class I (low risk)
Regulation
21 CFR 890.5925
Specialty
Physical Medicine

Other 510(k)s with product code ILZ

510(k)DeviceApplicantDecision
K921711Flexion Distration SupportILZ · Traditional Altoona Medical Supply07/13/1992SE
K895382Vibra-Trac Traction TableILZ · Traditional Vibra-Trac Industries10/16/1989SE
K884340AMX-110, Amx-Ii and Amx-IiiILZ · Traditional Dyna-Med01/24/1989SE
K852398Vector Bar Suspension/Traction UnitILZ · Traditional Powlan Manufacturing Co.08/12/1985SE
K844490Traction AccessoriesILZ · Traditional Jerome Medical02/21/1985SE
K831135Saunders #7080 Cervical Traction SysILZ · Traditional Chattanooga Group, Inc.06/24/1983SE
K830245Head HalterILZ · Traditional Warm & Form, Orthopedic Materials03/09/1983SE
K823659Pelvic Traction BeltILZ · Traditional Warm & Form, Orthopedic Materials12/30/1982SE
K823166Pelvic Traction BeltILZ · Traditional Warm & Form, Orthopedic Materials11/10/1982SE
K791808Cervi-TracILZ · Traditional Dr. K.G. Rude10/01/1979SE

Questions and answers

When was Boger Auto-Traction Device cleared by the FDA?

Boger Auto-Traction Device (K820663) received a 510(k) decision of Substantially Equivalent on May 3, 1982, 54 days after the submission was received.

What is the product code of K820663?

The FDA product code is ILZ – Accessories, Traction, a Class I (low risk) device regulated under 21 CFR 890.5925.